cessna aircraft company aircraft division wichita, kansas … · 1997. 6. 1. · the cessna...
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CESSNA AIRCRAFT COMPANY
AIRCRAFT DIVISION
WICHITA, KANSAS 67277
A SUPPLIER’S GUIDE TO ACCEPTABLE DATA SUBMITTALS
REPORT NO: GEN-96-002
REPORT DATE: June 1, 1997
APPROVED BY: _____________________
R. Phillips
APPROVED BY: _____________________
R. Held
APPROVED BY: _____________________
L. Van Dyke
APPROVED BY: _____________________
L. Bitker
APPROVED BY: _____________________
P. Hughes
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P.O. Box 7704 A Supplier’s Guide to Acceptable Data Submittals
Wichita, KS 67277 Report Number: GEN-96-002 Rev. C
REVISIONS
LETTER DATE DESCRIPTION APPROVED
A 11-30-2000 FMECA replaced by SSA
Rev Date By: Approved By:
B 3/10/2015 See Separate Electronic
Signature Sheet
See Separate Electronic Signature
Sheet
ECR No: 099985
Section Description
Global Updated document format and fonts, and corrected spacing.
Table of
Contents
Updated page numbers and titles.
§1 Is “General Formatting - Reports…,” was “General Formatting…”
Is “Supporting Report/Data Submission Information…,” was “Support Report
Information…”
Is “…in nearly every data submittal or report…,” was “…in nearly every
report…”
§2 Added “- Reports” to section title.
Under ‘Binding,’ added “Electronic report submission is preferred. Reports
should be provided in a single electronic file. If paper submission is
necessary, …”
Under ‘Margins,’ added “Standard margins of 3/4" to 1 1/4” are acceptable.
For paper submissions, …”
Under ‘Page Numbering,’ added “…, with the exception of the title page,…”
Under ‘Page Size,’ added “…is preferred, but it is understood that some over-
sized pages may be necessary. For paper submissions,…”
§3 Added “/data submission” following “report” in the section title and in two
other locations.
Is “Section 3.1 describes the information that should be submitted with any
type of data. Sections 3.2 through 3.7 describe required components of
reports.” Was “These general sections include the information sheet, title
page, contents, and revisions page.”
§3.1 Added “/data submission” following report in two locations.
Is “The information shall include the following items:..,” was “The
information sheet shall include the following items (ref. Fig. 3.1–1):...”
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P.O. Box 7704 A Supplier’s Guide to Acceptable Data Submittals
Wichita, KS 67277 Report Number: GEN-96-002 Rev. C
Deleted “Document Type – identify as one of the following types:
ATP Acceptance Test Procedure, DTA Damage Tolerance Analysis
FAT Fatigue Analysis, QSR Qualification by Similarity, QTP Qualification
Test Procedures, QTR Qualification Test Results, RSP Reliability
Substantiation Plan, RSR Reliability Substantiation Results, SAR Stress
Analysis, SSA System Safety Assessment.”
Added “14. ECCN, 15. Model, 16. Notification of Change (Major or Minor).”
Added “Figure 3-1 shows Cessna Form 2473, which can be completed and
returned with electronic or paper data submissions. For electronic
submissions, suppliers may have the option of providing the required
information via electronic template. If an electronic template is not available,
the information must be provided as a separate sheet during the transmission
of data.”
Revised Figure 3.1-1 and caption.
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P.O. Box 7704 A Supplier’s Guide to Acceptable Data Submittals
Wichita, KS 67277 Report Number: GEN-96-002 Rev. C
Rev Date By: Approved By:
C Sept. 1,
2015
See Separate Electronic
Signature Sheet
See Separate Electronic Signature
Sheet
ECR No: 099985
Rev. C
Section Description
QSR Title
(Now) "QUALIFICATION BY SIMILARITY REPORT (QSR)",
(Was) "QUALIFICATION BY SIMILARITY (QSR)"
Purpose of this Document
(Remove) " This report does not present information on the procedures
required for the report—it is not a Qualification by Similarity Methods
guide."
Purpose of a Qualification by Similarity Report
(Now) "A Qualification by Similarity Report (QSR) is a report that shows
similarity of a new or modified part to a previously …"
(Was) "A Qualification By Similarity Report (QSR) is a report that seeks to
establish viable similarity to a previously …"
(Add) "A QSR may also include additional … has adequately been defined."
Overview of a Qualification by Similarity Report
(Now) "To minimize the qualification test effort, a QSR should be pursued
when it is determined that a valid similarity exists between the part being
proposed and an existing qualified part or component. This generally means
that the form, function, materials, and manufacturing methods, are the same.
Operating loads and environmental operating conditions may be no more
severe for the new part than for what the previously part was qualified to."
(Was) "A QSR may be pursued when it is determined that a viable similarity
exists between the part being proposed and an existing qualified part or
component. This generally means that the form, function, materials,
manufacturing methods, operating loads, and environmental operating
conditions between the two parts are similar."
(Add) "Analysis and design review are … to some other previously tested
part."
QSR 1.1 (Now) "This section is required to include …"
(Was) "This paragraph should include …"
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Wichita, KS 67277 Report Number: GEN-96-002 Rev. C
Rev. C
Section Description
QSR 1.2 (Now) "This section is required to include a brief description of the end
product being analyzed for this QSR including the Supplier and Cessna part
numbers of both the qualified part(s) and the part being qualified."
(Was) "This paragraph should include a brief description of the end product
being analyzed for this QSR including the contractor and Cessna part numbers
of both the qualified part and the part being qualified."
QSR 1.3 (Now) "This section is required to summarize …"
(Was) "This paragraph should summarize …"
QSR 2.0 (Now) "Summarize the report and include a brief …"
(Was) "Summarize the report and include an brief "
(Now) "If a requirement has been waived by Cessna Engineering, explicitly
state this."
(Was) "If a requirement has been waived, explicitly state this."
(Now) "Specify the military, federal, or industry specifications and standards
to which testing of the new part would be required …"
(Was) "Specify the military, federal, or industry specifications and standards
to which the testing is required …"
(Now) "Specify the military, federal, or industry specifications and standards
to which the testing is required … shall be summarized and included."
(Was) "A list of any tests still required to compensate for differences between
the two components or new tests required for qualification shall be included."
QSR 2.1 (Now) "This section shall document what is identical …
(Was) "This paragraph shall document the similarities …"
(Now) "… section …", (Was) "… paragraph …"
QSR 2.2 (Now) "… section …", (Was) "… paragraph …"- 2 places
(Now) "Provide either the justification that the difference does not invalidate
previous qualification data or state what additional qualification (analysis or
qualification testing) of the difference will be required."
(Was) "Describe how the differences affect the qualification criteria."
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Wichita, KS 67277 Report Number: GEN-96-002 Rev. C
Rev. C
Section Description
QSR 3.0 (Now) "This section shall document the rationale, data, analysis, and
justification for qualification by similarity analysis."
(Was) "This section shall document the rationale for qualification by
similarity."
(Remove) "Include any field service history that the unqualified component
may have, including any flight–time on preproduction aircraft as well as any
tests that the component has undergone. If possible, compare the results of
any similar tests between the two components."
(Add) "This section of the QSR is required … with any RTCA DO-160
qualification requirement."
QSR 4.0 Title
(Now) " QUALIFICATION TESTING",
(Was) "QUALIFICATION TEST"
QTP Purpose of this Document
(Remove) "This report does not present information on the procedures
required to setup or conduct a test—it is not a Qualification Test Procedures
Methods guide."
Purpose of a Qualification Test Procedure Report
(Now) "A Qualification Test Procedure (QTP) …"
(Was) "A Qualification Test Procedures (QTP) …"
(Now) "… provides test setup and instrumentation … show …"
(Was) "… seeks to establish …"
(Add) "… applicable …"
Overview of a Qualification Test Procedure Report
(Now) "… is required to …", (Was) "… should …"
(Now) "… shall …", (Was) "… must …"
QTP 1.1 (Now) "This section is required to …", (Was) "This paragraph should …"
QTP 1.2 (Now) "This section is required to …", (Was) "This paragraph should …"
(Add) "… that are applicable to this … shall be described and justified."
QTP 2.0 (Add) "A brief description of the component or system … definition of the
Test Article."
QTP 2.2 (Now) "… is required to …", (Was) "… should …"
(Now) "State if …", (Was) "It should be clear if …"
(Now) "… these are also required to be described."
(Was) "… these should be made clear."
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Rev. C
Section Description
QTP
2.2.1.1
(Now) "… are also required to …", (Was) "… should …"
QTP
2.2.1.2
(Now) "This section is required to present …"
(Was) "This section presents …"
QTP
2.2.2
(Now) "This section is required to present …"
(Was) "This section presents …"
(Add) "… Engineering …"
QTP 3.0 (Now) "The number of Test Articles … in the test report."
(Was) "Each test should be … criteria of each test should be clearly stated."
QTP 4.0 (Add) "In order to facilitate … and other data in the QTP."
(Now) "The test facilities, equipment, and instrumentation shall be …"
(Was) "The test facilities should be …"
(Now) "… is required to be tabulated or listed."
(Was) "… should be tabulated."
(Now) "This table is required to include equipment, and instrumentation
descriptions and model numbers or identification."
(Was) "This table should include description and model number or
identification."
(Now) "The QTP is required to … in the test procedures and not here."
(Was) "It is not necessary to identify the serial numbers of the equipment in
this report."
QTP 5.0 (Now) "If a Cessna ODA conformity inspection is required it shall be clearly
stated."
(Was) "If an FAA conformity is being performed it must be clearly stated."
(Now) "Test setups and instrumentation shall … the conformity status."
(Was) "The procedures to handle deviations to the design definition should be
identified."
QTP 6.0 (Now) "The test procedures are required … for performance of the tests."
(Was) "The individual tests should be … procedure should be listed."
(Add) "Any special calibration or adjustment … included in the test report."
(Remove) "Any special equipment … for using that equipment."
(Now) "Pass/Fail criteria shall be …", (Was) "Pass/Fail criteria should be …"
(Add) "For example, if the acceptance … specific scope of the QTP."
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Rev. C
Section Description
QTR Purpose of a Qualification Test Results Report
"A Qualification Test Results (QTR) defines the required testing needed to
establish that a vendor component meets all requirements specified in the
controlling engineering documents."
"A Qualification Test Results (QTR) is a report that documents the test results
which were the result of performing the test procedures defined in the QTP.
These results are used to establish that a vendor component meets all
requirements specified in the controlling engineering documents."
Overview of a Qualification Test Results Report
(Now) "The Qualification Test Results report is required to …"
(Was) "The Qualification Test Results should …"
QTR
Table of
Contents
(Add) " Scope and Objective
Requirements"
QTR 1.1 (Add) "1.1 Scope and Objective"
(Now) "This section shall …", (Was) "The introduction shall …"
QTR 1.2 (Add) "1.2 Requirements"
(Add) "This section is required to … to the following regulations:"
QTR 4.0 (Now) "… where the testing was accomplished and what equipment …"
(Was) "… where the testing was accomplished, what equipment …"
(Remove) ", and the name of a person to contact that can answer questions
regarding facilities, equipment, and how tests were run"
QTR 6.0 (Now) "Following is a list of typical data … passed each test section."
(Was) "If FAA conformity was required … 8100–1 if applicable."
QTR 7.0 (Add) "Even though it may be obvious … the Test Article with retest."
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Report: GEN–96–002, Rev C
A supplier’s guide to acceptable data submittals
TABLE OF CONTENTS
SECTION TITLE PAGE
1. INTRODUCTION....................................................................................................... 2
2. GENERAL FORMATTING - REPORTS .................................................................. 3
3. SUPPORTING REPORT/DATA SUBMISSION INFORMATION .......................... 4
3.1 Information Sheet ................................................................................................. 4
3.2 Title Page .............................................................................................................. 6
3.3 Revisions Page ..................................................................................................... 6
3.4 Table of Contents Page ........................................................................................ 6
3.5 References ............................................................................................................ 6
3.6 List of Abbreviations and Symbols ...................................................................... 6
3.7 List of Definitions ................................................................................................ 6
4. ACCEPTED REPORT FORMATS ............................................................................ 7
Acceptance Test Procedure (ATP) .......................................................................... 7
Damage Tolerance Analysis (DTA) ...................................................................... 10
Fatigue Analysis (FAT) ......................................................................................... 16
System Safety Assessment (SSA) ......................................................................... 21
Qualification By Similarity (QSR) ........................................................................ 28
Qualification Test Procedure (QTP) ..................................................................... 33
Qualification Test Results (QTR) ......................................................................... 39
Reliability Substantiation Plan (RSP) ................................................................... 43
Reliability Substantiation Results (RSR) .............................................................. 47
Stress Analysis (SAR) ........................................................................................... 51
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P.O. Box 7704 A Supplier’s Guide to Acceptable Data Submittals
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1. INTRODUCTION
A wide range of engineering documents supporting supplier parts and equipment is
regularly received and reviewed by Cessna’s engineering department. In the absence of
any pre–defined format requirements, the review process can be cumbersome and
inefficient for both Cessna as well as the submitting supplier. This report presents
acceptable formats for the more common document types.
While certain content requirements cannot be avoided—and indeed, formatting and
content go hand–in–hand—it is the primary intention of this report to define only the
layout and formatting needs of submitted data. The specific subjects to be covered, and
the data to be included, will generally be defined in the specification control documents
provided by Cessna. These specifications will always take precedence over any
requirements contained in this document.
Many companies have report formatting standards that have been accepted by Cessna in
the past and strict compliance with this standard is not required for data to be approved.
Nonetheless, compliance will ensure uniformity with data submittals from other sources
and will aid Cessna in our evaluation. To avoid conflicts, it is suggested that deviations
from this standard be approved by Cessna prior to document submittal.
This report divides the formatting requirements into three categories:
General Formatting - Reports (Section 2) defines the very basic formats of page size,
margins, font size, and so on.
Supporting Report/Data Submission Information (Section 3) defines the report sections
that would be expected in nearly every data submittal or report, i.e. Information Summary
Sheet, Reference Page, Table of Contents, and the like.
Acceptable Report Formats (Section 4) is the principal source for the specific format
requirements for each document covered in this report.
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2. GENERAL FORMATTING - REPORTS
General Formatting affects the overall “look” of the report. The goal is to provide an
easy–to–read document in which data can be presented clearly and uniformly from one
document to the next.
Binding Electronic report submission is preferred. Reports should be
provided in a single electronic file. If paper submission is
necessary, there is no preference towards any single binding
method. It is acceptable (and most common) to submit reports in
standard loose–leaf, three–ring folders
Character Fonts For the general narrative, fonts smaller than 10 pt are discouraged.
Fonts smaller than 10 pt may still be used for figures, tables, or
other areas if their use improves readability by condensing
information that would otherwise be split across several pages to be
printed on a single page. Hand–written report sections are
sometimes inevitable (e.g., as in recorded data sheets from tests).
For these cases, the document should be legible and of adequate
quality for subsequent copies. In any case, the document must be
readable after being reproduced on typical photocopy equipment.
Figures and Tables Any figure or table reference in the report text must be numbered
and labeled. The preferred orientation is portrait.
Headers Each page shall include the supplier name, as well as the document
number.
Language English
Line Spacing Double–spaced typed
Margins Standard margins of 3/4" to 1 1/4” are acceptable. For paper
submissions, at least 1 1/4” margin at the binding and 3/4” margins
along all other edges. The margin at the binding shall be sufficient
to allow photocopying of permanently bound documents.
Page Numbering Each page, with the exception of the title page, shall be numbered.
Page Size 8 ½” x 11” is preferred, but it is understood that some over-sized
pages may be necessary. For paper submissions, all fold–outs
should be such that they fold within the standard page size.
Page Color White
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3. SUPPORTING REPORT/DATA SUBMISSION INFORMATION
Certain sections of a report/data submission are required regardless of the report/data
submission content. Section 3.1 describes the information that should be submitted with
any type of data. Sections 3.2 through 3.7 describe required components of reports.
3.1 Information Sheet
A report/data submission information page shall be included with each report/data
submission. This single sheet defines all relevant information about the report to ensure
proper coordination with the reviewing engineers and other project support personnel.
The information shall include the following items:
1. Company Name – The name of the submitting supplier—this may not be the same as
company that actually wrote the report.
2. CAGE – Commercial and Government Entity code of the controlling supplier. If not
known, enter N/A.
3. Document Number – As defined by the supplier.
4. Document Revision
5. Document Title – As defined by the supplier
6. Part Number – List the supplier part number(s) that are associated with this report
7. Associated Cessna Part Number(s)
8. Reference Cessna Documents – List any documents that have been referenced.
9. Purchase Order/Contract No.
10. Authors – point of contact for possible questions
11. Phone/Address
12. Date Submitted
13. Abstract – contains a brief summary of the report contents
14. ECCN
15. Model
16. Notification of Change (Major or Minor)
Figure 3.1-1 shows Beechcraft Form 900-33769, which can be completed and returned
with electronic or paper data submissions. For electronic submissions, suppliers may
have the option of providing the required information via electronic template. If an
electronic template is not available, the information must be provided as a separate sheet
during the transmission of data.
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FIGURE 3.1–1 Summary Information Sheet
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3.2 Title Page
The Title Page shall include, as a minimum, the following information:
1. Company Name and CAGE
2. Document Name
3. Document Number
4. Purchase Order/Contract No.
3.3 Revisions Page
All report revisions shall be detailed on the revision page. In addition, a brief description
of the nature of the revision may be helpful.
3.4 Table of Contents Page
Each of the major sections along with most of the minor subsections shall be included in
the table of contents. The specific formats for each report–type (as given in Section 4)
present a general guideline to be followed.
3.5 References
Any source used in the report shall be listed on the reference page. In most cases this
would include the relevant federal regulations, any Cessna documents used, the source for
material properties, and any in–house documents used.
3.6 List of Abbreviations and Symbols
All symbols and abbreviations used throughout the report shall be listed. Exceptions can
be made when the abbreviation used is either obvious within context, or is in common
usage (such as FAA or NASA).
3.7 List of Definitions
It is anticipated that for most reports this section will not be required; however,
sometimes words are used with a specific meaning that might otherwise be
misinterpreted. For instance; in certain usage the word “Flight” can mean any number of
takeoffs and landings from engine start to shut–down, whereas in a fatigue usage, the
word “Flight” encompasses only a single takeoff and landing, each touch–and–go is
therefore a “Flight.” This section shall contain a list of those items that have specific or
peculiar meaning in the context of the report.
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P.O. Box 7704 A Supplier’s Guide to Acceptable Data Submittals
Wichita, KS 67277 Report Number: GEN-96-002 Rev. C
4. ACCEPTED REPORT FORMATS
This section presents report outlines or skeletons that define an acceptable report layout
for the more common report-types. These outlines are intended to be general in nature so
as to allow the supplier the flexibility needed to meet the special needs of individual
reports. Each outline is preceded by a brief description of the purpose of the report, an
overview of the report content, and a document outline presented in the form of a typical
table of contents.
The reports presented, and their respective report codes are as follows:
ATP Acceptance Test Procedure
DTA Damage Tolerance Analysis
FAT Fatigue Analysis
QSR Qualification by Similarity
QTP Qualification Test Procedures
QTR Qualification Test Results
RSP Reliability Substantiation Plan
RSR Reliability Substantiation Results
SAR Stress Analysis Report
SSA System Safety Assessment
ACCEPTANCE TEST PROCEDURE (ATP)
Purpose of this Document
This document presents acceptable format and minimum content requirements for an
Acceptance Test Procedure. This document does not present information on the
procedures required for any test procedures—it is not an Acceptance Test Procedures
Methods guide.
Purpose of an Acceptance Test Procedure Report
An acceptance test is performed on components to verify that the production components
fulfill the requirements of the design activity and/or certifying agency under which it is
being purchased. The parameters being measured should include physical dimensions
and weight of the component as well as operational performance. An Acceptance Test
Procedure (ATP) is a document that establishes the procedures used to determine that
production components meet those requirements specified in Cessna’s Source Control
Document including all referenced Federal Aviation Regulations.
Overview of an Acceptance Test Procedure Report
An acceptable Acceptance Test Procedures report will identify all parameters that are to
be tested and the manner in which the test will be performed. The level of performance
(pass/fail criteria) for each individual test must be clearly stated.
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How to use this Document
The following pages are organized as a full Acceptance Test Procedure. The
accompanying text for each section describes the expected content along with notes on
formatting. The pages are listed sequentially; however, in an actual report a page
numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2, ...) is
usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of an
Acceptance Test Procedure.
TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Scope and Objective
Requirements
2.0 REFERENCE DOCUMENTS
Government Documents
Non–Government Documents
3.0 SUMMARY OF TESTS
4.0 TEST FACILITIES AND EQUIPMENT
5.0 INSPECTION AND CONFORMITY
4.0 TEST PROCEDURES
1.0 INTRODUCTION
1.1 Scope and Objective
This paragraph should include a brief description of the scope and objective of this
document. This should include identifying the component being tested and the
specification requirements to which it is being tested.
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1.2 Requirements
This paragraph should clearly state to what specification control document the component
is being tested.
2.0 REFERENCE DOCUMENTS
This section should tabulate all applicable documents. The criteria for determining the
applicable revision levels of the documents should also be clearly stated.
2.1 Government Documents
This section should list all applicable government standards.
2.2 Non–Government Documents
This section should list all applicable Cessna and supplier documents.
3.0 Summary of Tests
Each test should be tabulated. The objective and the passing criteria of each test should
be clearly stated as well as the passing criteria.
4.0 TEST FACILITIES AND EQUIPMENT
The test facilities should be identified in this section. This includes outside laboratories
and their available equipment. All equipment used in the testing should be tabulated.
This table should include description and model number or identification. It is not
necessary to identify the serial numbers of the equipment in this section of the document.
If necessary, any applicable equipment serial numbers may be listed on the data sheets.
Additionally, there should be a clear statement as to how the recorded data will be
maintained and for what length of time the data will be maintained.
5.0 INSPECTION AND PART CONFORMITY
This section shall clearly state that the part or system has been inspected and conforms to
the design definition. All deviations to the design definition should be documented in the
appendix on the appropriate forms.
6.0 TEST PROCEDURES
The individual tests should be fully described here along with the step–by–step procedure
for each. Any special equipment required during a test should be clearly stated, as well as
any instructions for using that equipment. Sample data sheets should also be included for
the approval phase of this document. Pass/Fail criteria should be clearly stated in the text
as well as on the face of the data sheet.
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DAMAGE TOLERANCE ANALYSIS (DTA)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
Damage Tolerance Analysis report. This report does not present information on the
procedures required for the analysis—it is not a Damage Tolerance Methods guide.
Purpose of a Damage Tolerance Analysis
A Damage Tolerance Analysis (DTA) is a structural analysis done to identify and
substantiate the inspection intervals required to ensure adequate safety. This guide is
applicable to a crack growth analysis supported by a residual strength analysis for the
critical crack (flaw) length. The Damage Tolerance Analysis is separate from a Fatigue
Analysis—generally associated with a safe–life, or life–limited part.
Overview of a Damage Tolerance Analysis
The general steps for a DTA include
1. Selection of critical locations
2. Stress history from load spectrum
3. Crack growth analysis
4. Residual strength (critical crack length)
5. Inspection requirements
How to use this Document
The following pages are organized as a full Damage Tolerance Analysis report. The
accompanying text for each section describes the expected content along with notes on
formatting. The pages are listed sequentially; however, in an actual report a page
numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2, ...) is
usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a
Damage Tolerance Analysis report. Depending on the specific requirements of each
analysis, some modifications would be appropriate. For instance, if two independent and
unrelated assemblies were being covered in the same report, with several analysis
locations on each assembly, then it might make sense to repeat sections 3.0 through 7.0
for each assembly. In any event, the outline presents the major topics that are expected in
all reports.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Locations Analyzed
Certification Requirements
2.0 SUMMARY OF INSPECTION REQUIREMENTS
3.0 PART DESCRIPTION
4.0 SPECTRA
Operation Spectrum
Load/Stress Spectrum
Limit Load
5.0 MATERIAL PROPERTIES
6.0 ANALYSIS METHOD
Stress Intensity Solutions
Initial Flaw Assumptions
Spectrum Manipulations
Crack Growth Computer Code Used
7.0 CRACK GROWTH AND RESIDUAL STRENGTH
ANALYSIS
Location #1
Location #2
Location #3
1.0 INTRODUCTION
The introduction should include a brief summary of what the part is, why it is being
analyzed, what area of the part is analyzed, and what the final results are. The minimum
inspection interval should be listed along with the inspection method assumed in the
analysis.
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1.1 Locations Analyzed
This section shall present a summary of each of the locations with a brief description of
each one. It is often helpful to include an overall picture of the part with locator arrows to
the analyzed locations. Section 3 will present a description of the overall part being
analyzed. A full detail description of the analysis locations will be presented in Section 7
including the reasons for selections.
1.2 Requirements
If the part is to be certified to particular Damage Tolerance requirements, then the
applicable paragraph numbers shall be listed—i.e., FAR 25.571(b). If additional
requirements are being met, including Cessna requirements, then those shall be listed
also.
2.0 SUMMARY OF INSPECTION REQUIREMENTS
At least two types of inspection are expected—initial and recurring. These inspection
times are dependent on the inspection method assumed, and when appropriate, the
inspection intervals for different inspection techniques should be presented as well. In
some cases, the time to initial inspection may be found to be extremely long (no crack
growth) and may be stated as such.
3.0 PART DESCRIPTION
It is helpful to include a reasonably thorough description of the part being analyzed
including its relationship to the surrounding area of the aircraft. Illustrations clearly
showing part orientation should be included.
4.0 SPECTRA
The spectra refers to the history of cyclic loads or stresses that the analyzed part
undergoes during its assumed lifetime. The stress intensity history used for the crack
growth analysis is defined by the global operational profile, the load spectrum, and the
local stresses.
4.1 Operation Spectrum
The operational spectrum is defined by the usage of the aircraft—flight length, altitude,
speed, etc., and will usually be defined by Cessna. Except in a few special cases, the
flight profiles that any single aircraft, or fleet of aircraft, will fly can only be generally
approximated. In many cases, a single general flight profile can be assumed using the
expected hours per flight as the basis, while in other cases several distinct flight profiles
may be combined according to their expected number of occurrences.
4.2 Load/Stress Spectrum
The load spectrum defines the cyclic loading that the aircraft sees during flight and
ground operations. The stress spectrum derives directly from the load spectrum, but is in
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terms of stress, not load. The load spectrum is often defined in terms of a load
exceedance curve. For instance, the maneuver load spectrum may be given in terms of an
exceedance curve of aircraft center–of–gravity load factor. If a continuous exceedance
curve has been converted to a few discrete steps, the procedure used should be defined
here.
For analyses with multiple locations, it is sufficient to present only an overview of the
load spectrum here, and to present the detailed stress spectrum in Section 7 for each
location. In any case, the actual stress spectrum used for the analysis shall be presented
either in the report body, or in an attached appendix. Any manipulations made to the
stress spectrum shall be covered in Section 6.
4.3 Limit Load
The critical crack length will be defined by the limit load case. The limit load level will
probably be greater than the largest spectrum load case, although in some cases the
maximum spectrum load will also be the limit load. As the critical case for residual
strength does not necessarily correspond to the critical case for static strength, the actual
case used should be clearly noted.
5.0 MATERIAL PROPERTIES
A complete listing of the relevant material properties used in the analysis along with their
source is required here. A typical list would be expected to include:
Fty yield strength
Ftu ultimate tensile strength
Kc plain–stress fracture toughness
Kic plain–strain fracture toughness
da/dN vs. ΔK crack growth rate data. Depending on the method of analysis used,
this information may be in the form of coefficients for any of several
possible equation forms, or in the form of tabular data for different R–
ratios.
ΔK Threshold
Constants
threshold below which there is no further crack growth.
R–cutoff stress ratio value, R, beyond which there is no further effect on crack
growth from changes in stress ratio.
If load interaction is accounted for in the analysis, or if further modifications to the crack
growth rate are used, then the applicable values shall be listed here as well.
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6.0 ANALYSIS METHODS
An overview of the analysis method shall be presented here. It is likely that in most
cases, linear fracture mechanics will be used (LEFM) along with widely accepted stress
intensity solutions and analytical techniques. Even so, it is important that these methods
be stated up–front to avoid any confusion with the final results.
Initial Flaw Assumptions
The initial flaw size can be dependent on several factors including manufacturing
procedures, part size, and type of part. However, typically, an initial flaw size of 0.05” is
used for edge cracks. An explanatory drawing is especially helpful when presenting the
initial flaw sizes used.
Load Interactions and Spectrum Manipulations
A wide range of load interaction models are available. The specific one used (if any)
must be presented along with any additional assumptions used in its use. The stress
spectrum loading order can have a significant effect on the final outcome. The method
used (range–pair, rain–flow, etc.) must be referenced as well. If the techniques used are
generally well known (Willenborg load interaction for instance), there is no need to go
into further detail.
Stress Intensity Solutions
An overview of the stress intensity solutions used in the analysis is presented here.
Virtually any stress intensity solution involves a series of assumptions and
approximations. If a compounding approach has been used, the compounded, individual
solutions should be referenced. Any in–house or commercial software used should be
listed.
Crack Growth Computer Code Used
The specific crack growth computer code shall be listed here. Since most of the available
crack growth software packages have very similar names, to avoid confusion the principle
authors of the software along with the release date (or version) should be listed as well.
7.0 CRACK GROWTH AND RESIDUAL STRENGTH ANALYSIS
This Section contains the actual detailed analysis of each location. The specific details of
the general methods listed in Section 6.0 should appear here. Additionally, the following
items would be expected in every analysis:
1. Logic used to select the critical locations analyzed. Some of the factors that would
cause a particular location to be chosen include high stresses, high stress
concentration factors, high load transfer, or field experience.
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2. The technique used to develop the stress distribution—Finite Element, Hand
Calculations, Strain Gauges, Photo Elastic, etc. The stress distribution has a direct
affect on the stress intensity solution.
3. Crack Growth Curves. These curves should clearly show the assumed initial flaw
size, the critical flaw size, various phases of crack growth (ligament, back side of
hole, etc.), and inspection times.
4. Inspection limits, including the minimum inspectable crack length and the inspection
technique used. These limits can usually be shown on the crack growth curves.
5. Critical Crack Length. Residual strength curves may be helpful in showing this.
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FATIGUE ANALYSIS (FAT)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
Fatigue Analysis report. This report does not present information on the procedures
required for the analysis—it is not a Fatigue Analysis Methods guide.
Purpose of a Fatigue Analysis
A Fatigue Analysis is a structural analysis done to identify and substantiate the safe–life
(or replacement life) required to ensure adequate safety. The Fatigue Analysis is separate
from a Damage Tolerance Analysis—generally associated with the determination of
inspection intervals.
Overview of a Fatigue Analysis
A fatigue analysis investigates the reduction in strength of a part, through the onset of
cracks, over the life of repeated load cycles. The general steps for a Fatigue Analysis
include:
1. Selection of critical locations
2. Stress history from load spectrum
3. Selection of appropriate life curves and scatter factor
4. Fatigue life analysis using the accumulation of damage (or other theory of fatigue
damage)
How to use this Document
The following pages are organized as a full Fatigue Analysis report. The accompanying
text for each section describes the expected content along with any other notes on
formatting. The pages are listed sequentially; however, in an actual report a page
numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2,...) is
usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a Fatigue
Analysis report. Depending on the specific requirements of each analysis, some
modifications would be appropriate. For instance, if two independent and unrelated
assemblies were being covered in the same report, with several analysis locations on each
assembly, then it would make sense to repeat sections 3.0 through 7.0 for each assembly.
In any event, the outline presents the major topics that are expected in all reports.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Locations Analyzed
Certification Requirements
2.0 SUMMARY OF FATIGUE LIFE
3.0 PART DESCRIPTION
4.0 SPECTRA
Operation Spectrum
Load/Stress Spectrum
5.0 MATERIAL PROPERTIES
Ultimate and Yield Strength
Fatigue Life Properties
6.0 ANALYSIS METHOD
Spectrum Manipulations
Fatigue Analysis Computer Code Used
7.0 FATIGUE ANALYSIS
Critical Location Selection Criteria
Location #1
Location #2
Location #3
1.0 INTRODUCTION
The introduction will include a brief summary of what the part is, why it is being
analyzed, what area of the part is analyzed, and what the final results are. Any calculated
safe–life limitations should be listed. The final numbers should be presented so as to
avoid any possible misinterpretation concerning the presence or lack of scatter factors.
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1.1 Locations Analyzed
This section shall present a summary and brief description of each of the locations. It is
often helpful to include an overall picture of the part with locator arrows to the analyzed
locations. Section 3 will present a description of the overall part being analyzed. A full
detail description of the analysis locations will be presented in Section 7 including the
reasons for selections.
1.2 Requirements
If the part is to be certified to particular fatigue–life requirements, then the applicable
paragraph numbers shall be listed—i.e., FAR 25.571(c). If additional requirements are
being met, including Cessna requirements, then those shall be listed also.
2.0 SUMMARY OF FATIGUE SAFE–LIFE
The final fatigue safe–life will generally be defined by the mean fatigue life divided by an
appropriate scatter factor. The values listed in this section are summarized from the
calculations given in section 7.
3.0 PART DESCRIPTION
It is helpful to include a reasonably thorough description of the part being analyzed
including its relationship to the surrounding area of the aircraft. Illustrations clearly
showing part orientation should be included.
4.0 SPECTRA
The stresses used for the fatigue analysis are defined by the global operational spectrum,
the load spectrum, and the local stresses.
4.1 Operation Spectrum
The operational spectrum is defined by the usage of the aircraft—flight length, altitude,
speed, etc., and will usually be defined by Cessna.
4.2 Load/Stress Spectrum
The load spectrum is often defined in terms of a load exceedance curve. For instance, the
maneuver load spectrum may be given in terms of an exceedance curve of aircraft center–
of–gravity load factor. If a continuous exceedance curve has been converted to a few
discrete steps, the procedure used should be defined here. For analyses with multiple
locations, it is sufficient to present only an overview here, and to present the detailed
stress spectrum in Section 7 for each location. In any case, the actual stress spectrum
used for the analysis shall be presented either in the report body, or in an attached
appendix. Any manipulations made to the stress spectrum shall be covered in Section 6.
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5.0 MATERIAL PROPERTIES
A complete listing of the relevant material properties used in the analysis along with their
source is required here. A typical list would be expected to include:
Fty yield strength
Ftu ultimate tensile strength
σ/n , ε/n. stress–life or strain–life (s–n) curves that define the cyclic fatigue life
for the material analyzed.
As it is unlikely that the geometry and material used to generate the fatigue–life curves
will be identical to the analysis location, it is important that the test coupon definition
used to develop the material data be listed. All s–n curves used in the analysis should be
presented in this section, or in an Appendix.
6.0 ANALYSIS METHODS
An overview of the analysis method shall be presented here. It is likely that in most
cases, some form of Miner’s rule of accumulated damage in combination with s–n curves
will be used. However, as there are a wide variety of variations on this method in use, it
is important that the full procedure be presented.
Spectrum Manipulations
Unless the spectrum consists of a simple constant amplitude cyclic loading, it is likely
that some modifications will need to be made to the stress spectrum prior to the analysis.
The stress ranges for each cycle are often re–arranged (cycle–counting) to ensure that the
analysis more closely reflects the true loading. Additionally, the Ground–Air–Ground
(GAG) cycle is typically identified as a separate load cycle in the spectrum.
Stress Concentration Factors
For most cases, s–n curves for a given material are presented for specific stress
concentration (Kt) values. The method used to determine the Kt used should be
presented as well as the rationale for using a particular s–n curve.
Fatigue Analysis Computer Code Used
For all but the simplest cases, the fatigue analysis will require the use of computer
programs. Whether an in–house program is used, or commercial software, a description
of the code should be included here.
7.0 FATIGUE ANALYSIS
This Section contains the actual detailed analysis of each location. The specifics of the
general methods listed in Section 6.0 should appear here. Additionally, the following
items would be expected in most every analysis:
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1. Logic used to select the critical locations analyzed.
2. The technique used to develop the stress distribution — Finite Element, Hand
Calculations, Strain Gauges, Photo Elastic, etc.
3. Stress Concentration (used in the selection of s–n curves)
4. Any additional factors
5. Scatter Factor justification or other method to account for variability.
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SYSTEM SAFETY ASSESSMENT (SSA)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
System Safety Assessment (SSA) report. Although information is given concerning the
content of a SSA, this report does not present the complete procedures required for the
analysis—it is not a SSA Methods guide.
Purpose of a System Safety Assessment Report
The System Safety Assessment (SSA) as required by Cessna is a procedure by which the
systematic, comprehensive evaluation of the implemented system (component) is
accomplished to show that relevant safety requirements are met. The SSA is to be
accomplished in accordance with the requirements and format of SAE ARP 4761,
Guidelines and Methods for Conducting the Safety Assessment Process on Civil Airborne
Systems and Equipment. The supplier prepared SSA integrates the results of the various
supplier prepared analyses to verify the safety of the overall system and to cover all the
specific safety considerations identified in those analyses.
How to use this Document
The following pages are organized as a full SSA report. The accompanying text for each
section describes the expected content along with notes on formatting. The pages are
listed sequentially; however, in an actual report a page numbering system that makes
reference to the Section number (i.e., 3.1, 4.1, 4.2,…) is usually preferred.
Document Outline
The figure below (presented as a Table of Contents ) gives the general outline of a System
Safety Assessment report.
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TABLE OF CONTENTS (TYPICAL)
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
2.0 REFERENCES
3.0 DESCRIPTION SUMMARY
4.0 SYSTEM SAFETY REQUIREMENTS AND
EVALUATION
4.1 System Safety Requirements and Evaluation
4.1.1 System Safety Design Requirements Source
Data
4.1.2 System Safety Design Requirements
Compliance Evaluation
4.1.3 Failure Condition Classification Validation
4.1.4 Verification of Safety Requirements
Compliance
4.1.5 Verification of CCA Safety Requirements
Compliance
4.2 SSA Documentation
5.0 SAFETY REQUIREMENTS VERIFICATIONS
(CONCLUSTIONS)
1.0 INTRODUCTION
This section contains a short description of the purpose of the document, what it is
intended to accomplish, and the system being analyzed.
2.0 REFERENCES
This section lists the documentation which will be used to form the basis of the analysis
to be accomplished. It includes, but is not limited to, the Cessna provided Source Control
Drawing (SCD); component Fault Tree Analyses (FTA), Dependence Diagrams (DD), or
Markov Analysis (MA); component Failure Modes Effects Analyses (FMEA) or Failure
Modes Effects Criticality Analysis (FMECA); SAE ARP 4761, SAE ARP 4754, RTCA
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DO-160D, RTCA DO-178B; the appropriate FAR/JAR sections (i.e., 25-1309) and the
appropriate FAA Advisory Circulars (i.e., AC 25-1309B), etc.
3.0 DESCRIPTION SUMMARY
This section consists of a detailed description (including the purpose) of the system(s)
being analyzed. It will include system block diagrams, input and output signal
descriptions, physical size (dimensions and weight), environmental conditioning
requirements, etc.
4.0 SYSTEM SAFETY REQUIREMENTS AND EVALUATION
These sections consists of the listing of the safety requirements being satisfied. The SSA
accomplishes the following:
a. Verification that the system safety design requirements established in the
component SCD are met.
b. Validation that the hazard classifications established by the supplier
analyses for the aircraft level effects are justified.
c. Verification that the design requirements identified in the supplier
accomplished Common Cause Analyses (CCA) are met.
4.1 System Safety Requirements and Evaluation
This section will discuss the sources of the system safety requirements which are to be
documented in this section of the SSA. Also discussed is the method suggested for
evaluation of the failure condition and requirements source data.
4.1.1 System Safety Design Requirements Source Data
This sub-section consists of a listing of the source data required accomplish the
evaluation required to be documented in the SSA. The types of source data to be
obtained include, but are not limited to, the following:
a. System architecture description and the associated design rationale.
b. Systems interfaces and their interactions with the items of the adjacent
systems.
c. Requirements and failure conditions identified in the component SCD.
d. List of functions and the associated rationale from the component SCD.
e. Common Cause Analyses results (as applicable):
(1) Zonal Safety Analysis (ZSA) results.
(2) Particular Risk Analysis (PRA) external threats.
(3) Common Mode Analysis (CMA) results.
f. Results of all the supplier developed supporting materials and lower level
studies required to accomplish the SSA. (Failure Mode Effects Analysis
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(FMEA)/Failure Modes Effects Summary (FEMS)/Failure Mode Effect
Criticality Analysis (FMECA), Fault Tree Analysis (FTA), etc.)
4.1.2 System Safety Design Requirements Compliance Evaluation
This sub-section lists each failure condition and documents how the safety design
requirements for that condition are complied with. Examples of the techniques which
may be used to accomplished the required evaluation are as follows:
a. Show, using Fault Tree Analysis (FTA), Dependence Diagrams (DD) or
Markov Analysis (MA), how items failures combine to lead to the
considered failure condition.
b. Show, using FTA, DD, or MA that qualitative and quantitative
requirements and objectives associated with the failure condition are met.
c. Notify Cessna Project Engineering of the “Not to Exceed” interval for
maintenance tasks driven by latent failures considered in the FTA, DD, or
MA which are required to be included in the appropriate drawings and
maintenance manuals. (Not all latent failures drive “Not to Exceed”
maintenance intervals.)
d. Verify that the development assurance level of items derived from the
FTA, DD, or MA have been met.
e. Test the condition to assure compliance with the requirements.
f. Demonstrate that the component performs as expected with the given
failure condition.
4.1.3 Failure Condition Classification Validation
This section lists the traceability between the requirements established in the component
SCD and the documentation which specifies the requirements to the design organizations.
The documentation includes but is not limited to the following:
a. Aircraft design requirements and objectives documentation.
b. System requirements documentation (if developed).
c. Test plans (ground tests, flight test, etc.).
d. Aircraft maintenance and flight manual inputs.
e. Common Cause Analyses documents.
4.1.4 Verification of Safety Requirements Compliance
This section defines how the system safety requirements identified in the component SCD
are complied with. The component SCD contains all the aircraft design requirements
along with the FAR/JAR requirements. The verification of compliance is accomplished
by one or more of the four standard means (i.e., test, analysis, demonstration and
inspection).
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4.1.5 Verification of CCA Safety Requirements Compliance
This section defines how the safety requirements developed by the CCA tasks (if
accomplished) are complied with. Examples of CCA requirements are as follows (list is
not all inclusive);
a. System and component separation and segregation (from the ZSA).
b. External threats (from the PRA).
c. Common mode failures (from the CMA).
The verification of compliance is accomplished by one or more of the four standard
means (i.e., test, analysis, demonstration and inspection).
4.2 SSA Documentation
This section defines the documentation which is required to be generated as part of the
SSA process. This is required in order to preserve the traceability of the steps taken in
the development of the SSA. The following data (list is not all inclusive) should be
preserved in order to maintain the required linkage between the source data used and the
SSA generated report:
a. Update failure condition list which includes the rationale showing
compliance with safety requirements (qualitative and quantitative).
b. Documentation showing how requirements for the design of the system
item’s installation (segregation, protection, etc.) have been incorporated.
These may include drawings, photographs, test reports, etc.
c. Materials used to validate the failure condition classification.
d. Safety maintenance tasks and associated “Not to Exceed” times.
e. Documentation showing how the system and items (including hardware
and software) have been developed in accordance with assigned
development assurance levels.
5.0 Safety Requirements Verifications (Conclusions)
This section consists of a table which indicates how each safety requirement was verified.
The first table below is an example of one approach for depicting the System Safety
Assessments results. The second table represents an alternate approach for depicting the
desired results.
System Safety Assessment
Item Number (1) Safety Requirement (2) Results (3) Verification Method &
Remarks (4)
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(1) The item number will be assigned by the supplier.
(2) This column is a copy of the Safety Requirements from the component
SCD. It will list the failure condition and the required level of safety.
(3) This column will show the level of safety the system is designed to meet
through analysis and testing. It will also show if the system design passes
or fails the required level of safety outlined in the Safety Requirements
column.
(4) Types of testing, analysis and all other necessary documentation numbers
that are used to show compliance to the safety requirements for that system
failure. This column will include reference to FTA or an FMEA that is
included in the body of the document. Component, and system testing
documents may be referenced in this column.
SYSTEM SAFETY ASSESSMENT SUMMARY – APPROACH ONE
Aircraft Function
Being Analyzed
(1)
1
Function
(2)
2
Item
No.
(3)
3
Failure
Condition
(Hazard
Description)
(4)
4
Phase
(5)
5
Effect of Failure
Condition on
Aircraft/Crew (6)
6
Classification (7)
7
Reference to
Supporting
Material (8)
8
Verification
(9)
(1) Title of the Component Level Function being analyzed (e.g., Component
Provides False Data).
(2) Description of the Function being analyzed (e.g., Component Provided
False Data Causes Aircraft to Fly in Hazardous Manner).
(3) An item number will be assigned to each functional failure condition
entry. This item number will serve as a means to correlate functional
failure conditions between reports.
(4) Description of the resulting hazard (e.g., Aircraft Flight Path Results in
Aircraft Crash).
(5) Phase of aircraft operation for the specific condition being analyzed (e.g.,
Landing or Rejected Takeoff (RTO)).
(6) Description of the effect the failure has on the aircraft/crew and the
resulting crew action to counteract the effects.
(7) The failure condition classification resulting from the occurrence of the
risk being analyzed (e.g., Minor, Major, Hazardous, Catastrophic).
(8) Listing of the reference material used to substantiate the action taken to
mitigate the failure effects.
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(9) The documentation used to verify the correctness of the analysis.
SYSTEM SAFETY ASSESSMENT SUMMARY – APPROACH TWO
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QUALIFICATION BY SIMILARITY REPORT (QSR)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
Qualification by Similarity Report.
Purpose of a Qualification by Similarity Report
A Qualification by Similarity Report (QSR) is a report that shows similarity of a new or
modified part to a previously certified or qualified part or component for the purpose of
reducing redundant and/or unnecessary testing requirements and expediting the
qualification effort.
A QSR may also include additional analysis or design review. The means of showing
compliance to each qualification requirement, design review, similarity analysis, or other
general form of analysis shall be clearly stated in the applicable QSR section. For the
purposes of this document, similarity means identicallity. Any design feature that is not
identical to that on the previously approved part shall be qualified by additional analysis
and/or test.
A QSR may be combined with a QTP, since the QSR is required to define the
qualification requirements for which similarity analysis is not valid and will require
testing. However, the QSR will be required to be submitted to Cessna at least in draft
form along with any supporting test data prior to Cessna Engineering approval of the QTP
for the new part. This is to ensure that any claim of similarity is valid and that the scope
of the test program has adequately been defined.
Overview of a Qualification by Similarity Report
To minimize the qualification test effort, a QSR should be pursued when it is determined
that a valid similarity exists between the part being proposed and an existing qualified
part or component. This generally means that the form, function, materials, and
manufacturing methods, are the same. Operating loads and environmental operating
conditions may be no more severe for the new part than for what the previously part was
qualified to.
Analysis and design review are strongly encouraged in lieu of qualification testing for
requirements where compliance is evident by review of design data or simple,
conservative analysis can be provided. For example, compliance with the Fluid
Susceptibility, Salt Fog, and Fungus Resistance requirements can be shown by review of
the materials and finishes used in construction of the component and by providing
handbook data or industry specifications showing the materials and finishes will not be
adversely affected by these threats. For most electromechanical components, compliance
with many of the electrical environment requirements can be addressed by design review
and analysis as equivalent means of satisfying the intent of electrical environment test
requirements. Explosion Proof qualification for an electrical component can be
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demonstrated if design review shows it has no commutation or arcing in normal operation
and analysis shows that any electrical heating can readily be dissipated so that surface
temperature limits are not exceeded at the highest approved operating temperature and
altitude.
With Cessna Engineering concurrence, analysis may also be provided to demonstrate that
a qualification requirement is not applicable to the particular design of the equipment.
Qualification test data for a previous similar part may be used if it meets the criteria of
FAA Order 8110.4C, Paragraph 2-6.k.(3). The data is required to show sufficient
evidence that the data was FAA approved, which may include conformity inspection
records, FAA or designee witnessing records, and/or other correspondence showing the
data was approved by a prior applicant. The QSR is also required to show that the data is
applicable to the new design. If the previously approved test data requires redacting of
proprietary data, the redacting cannot remove so much content that it is then not possible
to determine that the data is applicable to the new design.
Qualification by similarity analysis based on test data for a previously qualified part may
be shown only to a tested part. It is not acceptable to show similarity to a previous part
which was qualified only by being shown similar to some other previously tested part.
How to use this Document
The following pages are organized as a full QSR. The accompanying text for each
section describes the expected content along with any other notes on formatting. The
pages are listed sequentially; however, in an actual report a page numbering system that
makes reference to the Section number (i.e., 3.1, 4.1, 4.2,...) is usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a
Qualification by Similarity Report.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Scope and Objective
Part Description
Certification Requirements
2.0 SUMMARY OF SIMILARITY
3.0 RATIONALE FOR QUALIFICATION
4.0 QUALIFICATION TESTING
1.0 INTRODUCTION
1.1 Scope and Objective
This section is required to include a brief description of the scope and objective of this
document.
1.2 Part Description
This section is required to include a brief description of the end product being analyzed
for this QSR including the Supplier and Cessna part numbers of both the qualified part(s)
and the part being qualified.
1.3 Certification Requirements
This section is required to summarize all the qualification and certification requirements
listed in the contract, purchase order, control drawings, or governing regulations that are
applicable to this QSR. Cessna Engineering concurrence with the validity of similarity
claims and acceptability of any previously approved test data is required prior to QTP
acceptance to ensure the scope of the testing has been adequately defined. Cessna
Engineering will then provide the list of applicable regulations and their amendment
levels, which are required to be included in this section of the QSR with the statement:
"The data in this document is provided to support Cessna showing of compliance to the
following regulations:"
.
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2.0 SUMMARY OF SIMILARITY
Summarize the report and include a brief overview describing why this part should be
qualified by similarity. For each of the requirements listed in paragraph 1.3, describe in
detail how the test results for the previously qualified component will be similar/different
to the anticipated results for the unqualified component. If a requirement has been
waived by Cessna Engineering, explicitly state this. Specify the military, federal, or
industry specifications and standards to which testing of the new part would be required
to be performed and compare these with the specification/standards that the original
qualified component was tested. Provide justification why testing performed on the
previously qualified component meets the requirements of the specifications and
standards applicable to the new part. FAA AC 21-16G provides guidance for comparison
of the requirements of different revisions of RTCA DO-160. The means of showing
compliance to each qualification requirement, design review, similarity or other general
form of analysis, or new qualification testing shall be summarized and included.
2.1 Similarities
This section shall document what is identical between the new component and the
previously qualified component. This and the following section may be combined into a
single comprehensive table or section.
2.2 Differences
This section shall document the differences between the new component and the
previously qualified component. Provide either the justification that the difference does
not invalidate previous qualification data or state what additional design review, analysis,
or qualification testing of the difference will be required. This and the preceding section
may be combined into a single comprehensive table or section.
3.0 RATIONALE FOR QUALIFICATION
This section shall document the rationale, data, analysis, and justification for qualification
by similarity analysis. This section of the QSR is required to show that the previous part
has been reliable in its previous application. To state that there is no evidence of
unreliability does not show the part has been reliable and may only indicate poor keeping
of reliability data records. Even if similarity can be shown based on review of previously
approved qualification data, if a component has not demonstrated adequate reliability in
the previous similar application it will not be accepted for the new application without
redesign and additional qualification (test, analysis, and/or design review).
While review of service history is required to establish that the previously qualified part
has been reliable in service, use of service history alone is not acceptable for compliance
with any RTCA DO-160 qualification requirement.
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4.0 QUALIFICATION TESTING
Reference and briefly summarize the qualification test procedures and results for the
original part.
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QUALIFICATION TEST PROCEDURE (QTP)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
Qualification Test Procedure report.
Purpose of a Qualification Test Procedure Report
A Qualification Test Procedure (QTP) is a report that provides test setup and
instrumentation requirements, conformity inspection requirements (if for certification),
clear and concise step-by-step test procedures, and unambiguous, objective test result
acceptance criteria that will provide test data to show that a supplier component meets all
applicable requirements specified in the controlling engineering documents.
Overview of a Qualification Test Procedure Report
The QTP is required to identify all parameters that are to be tested and the manner in
which the test will be performed. The level of performance for successful passage of
each individual test shall be clearly stated.
How to use this Document
The following pages are organized as a full Qualification Test Procedures report. The
accompanying text for each section describes the expected content along with any other
notes on formatting. The pages are listed sequentially; however, in an actual report a
page numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2,...)
is usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a
Qualification Test Procedures Report.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Scope and Objective
Requirements
2.0 COMPONENT/SYSTEM DESCRIPTION AND
OPERATION
3.0 SUMMARY OF TESTS
4.0 TEST FACILITIES AND EQUIPMENT
5.0 INSPECTION AND CONFORMITY
6.0 TEST PROCEDURES
1.0 INTRODUCTION
1.1 Scope and Objective
This section is required to include a brief description of the scope and objective of this
document.
1.2 Requirements
This section is required to summarize all the qualification and certification requirements
listed in the contract, purchase order, control drawings, or governing regulations that are
applicable to this testing. Cessna Engineering concurrence with the validity of similarity
claims and acceptability of any previously approved test data is required prior to QTP
acceptance to ensure the scope of the testing has been adequately defined. Cessna
Engineering will then provide the list of applicable regulations and their amendment
levels, which are required to be included in this section of the QTP with the statement:
"The data in this document is provided to support Cessna showing of compliance to the
following regulations:"
The basis for the testing, such as an industry standard or general test specification, such as
RTCA DO-160 or MIL STD 810 shall be defined. Any deviation from the requirements
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of a general test specification on which the testing is based shall be described and
justified.
2.0 COMPONENT/SYSTEM DESCRIPTION AND OPERATION
A brief description of the component or system and its operation is required. It is not
necessary to provide detailed descriptive data in the QTP if reference is provided to other
documents where the detailed data can be found.
The QTP shall state the Part Number of the Test Article and the Assembly Drawing
number that defines it. It is not necessary to include revision level of the drawing, unless
the configuration of the test article can be determined only by reference to the particular
drawing revision level. An example of need to include a top Assembly Drawing revision
level is if significant changes are made during the testing to the design of the part by top
Assembly Drawing revision without change to the part number. If multiple Test Article
configurations are being tested or if changes occur during the testing and the differences
are defined only on lower level drawings that are not denoted on the top Assembly
Drawing, the differences in the design and in the lower level drawings shall be described
in this section as part of the definition of the Test Article.
2.1 Component/System Description
The physical characteristics of the component shall be described along with a summary of
its function.
2.1.1 Sub–Component Description
If the subject is a complex system it may be necessary to provide sub–component
descriptions. Additional sub-sections shall be added as needed.
2.2 Component/System Operation
This section presents a description of all operational aspects of the components. The
discussion is required to be written such that a person with minimal technical expertise
can understand how the component operates. State if there are manual and automatic
modes of operation. If the component has unique normal and abnormal operation modes,
these are also required to be described.
2.2.1 Normal Operation
2.2.1.1 Manual Operation Modes
This section presents a discussion of all manual operation modes. While automatic
operation modes would not be discussed here, any internal operations that are initiated
manually are also required to be discussed.
2.2.1.2 Automatic Operation Modes
This section is required to present a discussion of all automatic operation modes.
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2.2.2 Abnormal Operation
This section is required to present a description of any secondary or backup operational
features. It is acceptable to make reference to an existing document (and to supply to
Cessna Engineering) that discusses failure modes and other abnormal system operations.
3.0 SUMMARY OF TESTS
The number of Test Articles and the particular tests to be performed on each one shall be
defined. It is not necessary to identify the particular Test Article serial numbers, unless
different Test Article configurations will be required for different tests (for example,
assembly or adjustment to an extreme tolerance limit). It is generally undesirable to
identify Test Article serial numbers in a QTP, in case it becomes necessary to substitute a
different equivalent conformed part at the time of the test. Test Article serial numbers are
required to be recorded in the conformity records in the test report.
4.0 TEST FACILITIES AND EQUIPMENT
In order to facilitate preparation of the Conformity Inspection Request, the definitions of
the setup and instrumentation are required to be identified and segregated from test
procedures and other data in the QTP. The test facilities, equipment, and instrumentation
shall be identified in this section. This includes outside laboratories and their available
equipment. All equipment intended to be used in the testing is required to be tabulated or
listed. This table is required to include equipment, and instrumentation descriptions and
model numbers or identification. The QTP is required to either fully define the test
setups and instrumentation, or list drawings, layouts or specifications that define them. If
multiple tests are to be performed and each one requires a different setup, each setup
definition shall be identified and segregated from each other. Definition of test setup and
instrumentation shall be to the degree necessary to ensure that the intended function of
the setup and instrumentation can be verified by visual inspection during the Conformity
Inspection. The definition of the setup and instrumentation shall be sufficiently detailed
that their function could be duplicated based only on the definition in the QTP and
produce the same test results at any suitable test facility, without prior knowledge of the
intended results or reference to post test data or photographs.
The QTP shall specify the type, range, accuracy, sampling rate and any other significant
parameters required for the instrumentation. The QTP shall specify which parameters are
required to be recorded electronically and which ones may be hand recorded. Specifying
particular instrument part numbers should be avoided, since this would prevent
substitution of a suitable equivalent instrument at the time of the test. Specifying only the
part number of the instrument also impedes the ability of the Organization Delegation
Authorization (ODA) Unit Member (UM) witness and inspector to verify that the chosen
instrument is of suitable type, range, and accuracy at the time of the test without access to
manufacturer's data for the instrument. All instrumentation shall have current traceable
calibration and the calibration records are required to be available at the time of the
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Conformity Inspection. The locations and details of attachment of instrumentation taps
and probes can be defined by written description, but are required to be clear and precise.
All instrumentation shall include an allowable tolerance and that tolerance is required to
be accounted for in the specification of required test conditions.
Schematics shall be provided for test setup plumbing and wiring and shall reflect the
general layout required for the setup. Plumbing sizes and wire gauges shall be specified
if they are critical to function of the setup. Otherwise, at least the range of acceptable
sizes shall be specified. If particular locations of components in the setup are critical,
such as requiring a pressure gauge be plumbed as close to the test article as practical, that
should be noted on the schematic. Specific part numbers of components used in
construction of the setup, such as plumbing fittings, wire, switches, fasteners, etc…,
should not be specified, unless use of that particular part is essential to the required
function of the setup, as this may prevent substitution of another suitable part at the time
of the testing.
If multiple tests are to be performed and each one requires a different setup, each setup
definition shall be identified and segregated from each other.
The QTP shall include a statement that all instrumentation is required to be calibrated
prior to testing. Reference to the standard company QA procedures pertaining to
instrumentation calibration is normally acceptable. Reference to an industry standard
without defining means to accomplish it normally will not. Any special calibration
procedures that are required to be accomplished during the testing (such as zeroing
settings or selection of particular instrument range settings) shall be specified in the test
procedures and not here.
5.0 INSPECTION AND PART CONFORMITY
This section shall clearly state the level to which the part or system is being conformed.
If a Cessna ODA conformity inspection is required it shall be clearly stated. Test setups
and instrumentation shall be conformity inspected prior to performing the test. Any
deviation from the test setup and instrumentation definition in the QTP is required to be
approved by the Cessna ODA UM witness before the testing can begin. Any significant
change to the test setup and instrumentation may also require update to the conformity
record. Any special calibration or adjustment procedures that are required to be
accomplished during the testing (such as zeroing settings or selection of particular
instrument range settings) shall be specified in the test procedures rather than in the test
setup and instrumentation definition so that the changes required to be performed during
the testing will not affect the conformity status.
6.0 TEST PROCEDURES
The test procedures are required to be detailed to the degree that the procedure could be
successfully performed by any suitable test facility by any qualified personnel without
prior experience with the particular QTP or prior knowledge of the desired results. It is
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not acceptable to define test procedures solely by reference to a general test specification,
such as RTCA DO-160 or MIL STD 810. RTCA DO-160 defines general test
requirements and includes many options for performance of the tests.
Any special calibration or adjustment procedures that are required to be accomplished
during the testing (such as zeroing settings or selection of particular instrument range
settings) shall be specified in the test procedures. If the QTP specifies a particular setting
be used such as setting a power supply voltage, the actual setting used shall be recorded
with the data and included in the test report. Sample data sheets should also be
included. Pass/Fail criteria shall be clearly stated in the text as well as on the face of the
data sheet. For example, if the acceptance criteria for a proof pressure test is "There shall
be no detrimental permanent deformation", the QTP needs to define quantitatively how
much deformation is acceptable and how it is to be measured. Qualitative acceptance
criteria may also be used as long as they are unambiguous. If the QTP purpose is only to
take data for use in a subsequent analysis, the acceptance criteria shall be "Data shall be
taken."
All test conditions shall specify a bottom and top tolerance for each test parameter
(pressure, temperature, altitude, time, voltage, etc…). The test tolerances shall assume
worst case instrumentation tolerances. Additional tolerances may be required, depending
on the precision of the controls expected to be used for the test. For example, a pressure
transducer may have an accuracy of ±10 PSI, but the pressure regulator available for
performing the test may have a controllability of no better than ±50 PSI.
If the QTP contains additional "company" test requirements that are not required for
certification, they shall be suitably identified and segregated from the certification test
procedures. If additional certification testing is being performed that is in excess of that
necessary for the present certification program but is intended for use for certification of
future development airplanes, those procedures shall be identified as optional and
segregated from the procedures for the present certification program. Acceptance criteria
for additional, optional certification testing shall be specified as "Data shall be taken."
This is to ensure that if the optional test is failed or cannot be completed, it does not
interfere with the current certification program.
The QTP shall list the specific data required to be provided in the QTR. A typical data
requirements list is included in the QTR section of this document. That list may be
modified to match the specific scope of the QTP.
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QUALIFICATION TEST RESULTS (QTR)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
Qualification Test Results report. This report does not present information on the
procedures required for reducing test data—it is not a Qualification Test Results Methods
guide.
Purpose of a Qualification Test Results Report
A Qualification Test Results (QTR) is a report that documents the test results which were
the result of performing the test procedures defined in the QTP. These results are used to
establish that a vendor component meets all requirements specified in the controlling
engineering documents.
Overview of a Qualification Test Results Report
The Qualification Test Results report is required to identify all parameters that have been
tested and the manner in which the test was performed. The level of performance for
successful passage of each individual test must be clearly stated.
How to use this Document
The following pages are organized as a Qualification Test Results report. The
accompanying text for each section describes the expected content along with any other
notes on formatting. The pages are listed sequentially; however, in an actual report a
page numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2,...)
is usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a
Qualification Test Results Report.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Scope and Objective
Requirements
2.0 PART (OR SYSTEM) DESCRIPTION
3.0 SUMMARY OF TESTS
4.0 TEST FACILITIES AND EQUIPMENT
5.0 INSPECTION AND PART CONFORMITY
6.0 QUALIFICATION TEST RESULTS
7.0 CONCLUSION
1.0 INTRODUCTION
1.1 Scope and Objective
This section shall include a brief summary of the scope and objective of this document
regarding the applicable qualification testing.
1.2 Requirements
This section is required to summarize all the qualification and certification requirements
listed in the contract, purchase order, control drawings, or governing regulations that are
applicable to this testing. Cessna Engineering will provide the list of applicable
regulations and their amendment levels, which are required to be included in this section
of the QTR with the statement:
"The data in this document is provided to support Cessna showing of compliance to the
following regulations:"
2.0 PART (OR SYSTEM) DESCRIPTION
This section shall include a brief definition of the part or system and its operation.
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3.0 SUMMARY OF TESTS
This section shall summarize the testing and include an overview of the main problems, if
any, detected during or after the completion of the testing.
4.0 TEST FACILITIES AND EQUIPMENT
This section shall include a description of where the testing was accomplished and what
equipment was used for the testing.
5.0 INSPECTION AND PART CONFORMITY
This section shall provide a statement that the part or system has been inspected and the
part or system conforms to the design definition. If there are any non–conforming items,
they need to be listed with documentation supporting how they were approved for use in
the test.
6.0 QUALIFICATION TEST RESULTS
This section shall provide the results of each test, listing the test by controlling
engineering document paragraph number and Supplier qualification test procedure
paragraph number.
Following is a list of typical data requirements that are required to be provided in a QTR.
If there were multiple test sections each having different setups and conformity
documentation, the following data shall be organized in the Test Report according to each
section of the Test Procedure and clearly labeled as to which section of the Test
Procedure it applies to.
a) Photographs of each test setup, including any changes or adjustments made during
the testing.
b) Photographs of the Test Article before and after each test.
c) Results of physical examination of the Test Article and description of its
condition before and after each section of the testing, taking care to note any
conditions that may have existed prior to the testing.
d) Photographs of instrumentation locations.
e) Descriptions and photographs of any failures (if any).
f) Part numbers, serial numbers, range, nominal accuracy, and inspection dates of
instrumentation for each section of the testing.
g) List of witnesses for each section of the testing.
h) Times, dates and locations for each section of the testing.
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i) Cessna data approvals on FAA Forms 8100-9 and Conformity Inspection
Requests on FAA Forms 8120-10 for the Test Articles and Test Procedure, if the
testing was performed for certification purposes.
j) Conformity Inspection Records for the Test Articles, Test Setups, and
Instrumentation. These shall be organized according to each section of the Test
Procedure, if the testing was performed for certification purposes.
k) Recorded data, as specified in the Test Procedure. Typically:
1. Pressures, temperature, humidities, voltages, etc attained after required
elapsed times.
2. Actual durations at each test condition specified by the Test Procedure and as
applicable to the particular test.
3. Any instrument or control settings required to be set and verified in the Test
Procedure. Include the actual values, not just verification that they were set.
4. Ambient conditions in the lab at time of testing.
5. Observations of the test witnesses, even if recording them was not required by
the Test Procedure.
6. Any other data specified by the Test Procedure as required to be recorded.
l) List of deviations (if any) from required test setup, instrumentation or procedures.
If there were no deviations, this shall be stated. If the deviations were recorded by
"redline" markup to the QTP rather than being incorporated into the QTP by
revision, the redlines shall be included in the QTR.
m) Test failures and resultant corrective actions, if any.
n) Summary and conclusions as to whether the Test Article passed each test section.
7.0 CONCLUSION
This section shall state the justification for the part or system meeting the engineering
requirements. Even though it may be obvious from the test results, state the obvious.
The reader should not have to draw any conclusions of their own.
It will not be acceptable for any portion of the testing to have been failed and justification
provided that the failure was acceptable. Any test failures should have been coordinated
with Cessna Engineering and suitable disposition provided prior to completion of the
testing. Suitable dispositions that are required to be documented in the QTR would
include revision or redline deviation to the test procedure such that the Test Article
passed the changed QTP or corrective action and design change to the Test Article with
retest.
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RELIABILITY SUBSTANTIATION PLAN (RSP)
Purpose
This document presents an acceptable format and minimum content requirements for a
Reliability Substantiation Plan. This report does not present information on the
procedures required for the analysis—it is not a Reliability Methods guide.
Purpose of a Reliability Substantiation Plan
A Reliability Substantiation Plan (RSP) is part of a reliability program that the supplier
uses to propose a method for demonstrating that their components meet the required
reliability values prior to the first delivery of an aircraft with the specified equipment.
Overview of a Reliability Substantiation Plan
The general steps for a RSP include:
1. List agreed to reliability values/requirements
2. Describe system and environment
3. Selection of substantiation method
4. List components of final report
5. Provide schedule
How to use this Document
The following pages are organized as a full Reliability Substantiation Plan report. The
accompanying text for each section describes the expected content along with any other
notes on formatting. The pages are listed sequentially; however, in an actual report, a
page numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2, ...)
is usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a
Reliability Substantiation Plan report.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Scope and Objective
Reliability Values
2.0 SUMMARY
3.0 PART DESCRIPTION
4.0 ENVIRONMENT
5.0 DATA COLLECTION AND ANALYSIS
Field History
Testing
Schedule
1.0 INTRODUCTION
1.1 Scope and Objective
This paragraph should include a brief description of the scope and objective of this
document.
1.2 Reliability Values
This paragraph should include the reliability goal as listed in the Product Support
Agreement along with a brief description of how the goal was derived.
2.0 SUMMARY
Summarize the method you plan to use to substantiate reliability. This paragraph should
include the method used to demonstrate reliability. This could be field history or
reliability testing. Field history is the preferred method (assuming the design,
environment, and usage duty cycle are the same). If that information is often not
available, endurance testing and Highly Accelerated Life Testing (HALT) are two
effective methods for demonstrating reliability. Whatever method is selected, it must be
detailed in this plan and approved by Cessna Engineering before any reliability testing is
initiated.
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3.0 PART DESCRIPTION
This section describes the operation of the system and contains the details about the Line
Replaceable Unit (LRU). This may include block diagrams or any other information
pertaining to system or component description.
4.0 ENVIRONMENT
If testing is the means of substantiation, describe the test environment that the component
or system will be subjected to (as negotiated and agreed to with Cessna Engineering and
the Quality Engineering Reliability Department). This will include all testing parameters
that may include mission profile, environment, time, and units tested. If Highly
Accelerated Life Testing (HALT) is the method of substantiation, all stimuli shall be
described.
5.0 DATA COLLECTION AND ANALYSIS
5.1 Field History
Field history will be reported to Cessna Engineering to substantiate the reliability level
required. The initial report shall provide, but not be limited to, the following:
Part and Serial Number
Chart (Pareto) of Failure Modes
Identify Corrective Action Implemented
Service Bulletins
Modifications
Dates
Follow–up
Note: This substantiation report will be sent to Cessna Engineering within sixty days after
the design engineer’s request. This will give the Cessna sufficient time to determine if
any additional testing is required.
5.2 Testing
Failures will be reported to Cessna Engineering within 24 hours of failure occurrence.
The initial report shall provide, but not be limited to, the following:
Test log date
Part and Serial number
Test environment
Test elapsed time and number of cycles
Method of failure detection
Description of any other symptoms
Test Engineer name/signature
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Note: A written failure report will be sent to Cessna Engineering within 10 working days
of the occurrence.
5.3 Schedule
If testing is the means of substantiation, a test schedule shall be included with all major
milestones documented. Included with the schedule shall be a time period for
incorporating test induced corrective action.
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RELIABILITY SUBSTANTIATION RESULTS (RSR)
Purpose
This document presents an acceptable format and minimum content requirements for a
Reliability Substantiation Results report. This report does not present information on the
procedures required for the analysis—it is not a Reliability Methods guide.
Purpose of a Reliability Substantiation Results
A Reliability Substantiation Results (RSR) is part of a reliability program that a supplier
uses to demonstrate that their components have met the required reliability values prior to
the first delivery of an aircraft with the specified equipment.
Overview of a Reliability Substantiation Results
The general steps for a RSP include:
1. List agreed to reliability values
2. Describe system and environment
3. Selection of substantiation method
4. Provide final report
5. List engineering analyses and corrective action
How to use this Document
The following pages are organized as a full Reliability Substantiation Results report. The
accompanying text for each section describes the expected content along with any other
notes on formatting. The pages are listed sequentially; however, in an actual report, a
page numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2,...)
is usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a
Reliability Substantiation Results report.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Reliability Values
Substantiation Method
2.0 SUMMARY
3.0 PART DESCRIPTION
4.0 ENVIRONMENT
5.0 FAILURES AND CORRECTIVE ACTIONS
Field History
Testing
1.0 INTRODUCTION
1.1 Scope and Objective
This paragraph should include a brief description of the scope and objective of this
document.
1.2 Reliability Values
This paragraph should include the agreed to reliability value as listed in the Product
Support Agreement along with a brief description of how the goal was derived.
1.3 Substantiation Method
This paragraph should include the method used to demonstrate detailed in the Reliability
Substantiation Plan and be approved by Cessna.
2.0 SUMMARY
Summarize the level of component reliability substantiated. Provide an explanation if the
level of reliability substantiated is different from the value agreed to in the Product
Support Agreement (PSA). Discuss any prediction or testing anomalies that may have
occurred. Describe any changes to the original plan that may have taken place. Include
an overview of any failures. Describe any corrective actions taken. The summary shall
include conclusions and all recommendations based on the substantiation results.
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3.0 PART DESCRIPTION
This section describes the operation of the test system and contains details about the Line
Replaceable Unit(s) (LRU). This may include block diagrams or any other information
pertaining to system or component description.
4.0 ENVIRONMENT
If testing is the means of substantiation, describe the test environment the component or
system will be subjected to as negotiated and agreed to with Cessna Engineering and the
Quality Engineering Reliability Department. This will include all testing parameters that
may include mission profile, environment, time, and units tested. If Highly Accelerated
Life Testing (HALT) is the method of substantiation, all stimuli shall be described.
5.0 FAILURES AND CORRECTIVE ACTIONS
5.1 Field History
This section will include any failure modes and corrective actions taken place in the
component's history if this is the means of substantiation. This shall include, but not be
limited to, the following:
Part and Serial number
Chart (Pareto) of failure modes
Identify corrective action implemented
Service Bulletins
Modifications
Dates
Follow–up
5.2 Testing
If testing is the means for substantiation, all failures encountered during the reliability
testing shall be listed along with any corrective action required to reduce or eliminate
each failure mode encountered. This should include, but not be limited to, the following:
TEST
Test log date
Part and Serial number
Test environment
Test elapsed time and number of cycles
Method of failure detection
Description of any other symptoms
Root cause of failure
Test Engineer name/signature
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ANALYSIS
Analysis procedure
Root cause of failure
Other findings/secondary failures
Analysis Engineer name/signature
CORRECTIVE ACTION
Design change description
Process change description
Completion/implementation on product hardware
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STRESS ANALYSIS (SAR)
Purpose of this Document
This document presents acceptable format and minimum content requirements for a
Stress Analysis report. This report does not present information on the procedures
required for the analysis—it is not a Stress Analysis Methods guide.
Purpose of a Stress Analysis
A Stress Analysis is a structural analysis done to identify and substantiate critical parts
and/or part locations for adequate strength.
Overview of a Stress Analysis
The general steps for a stress analysis include:
1. selection of critical locations
2. application of external loads
3. development of stress model
4. calculation of internal stresses/loads
5. gathering of material properties (allowables)
6. calculation of strength margins
How to use this Document
The following pages are organized as a full Stress Analysis report. The accompanying
text for each section describes the expected content along with any other notes on
formatting. The pages are listed sequentially; however, in an actual report a page
numbering system that makes reference to the Section number (i.e., 3.1, 4.1, 4.2,...) is
usually preferred.
Document Outline
The figure below (presented as a Table of Contents) gives the general outline of a Stress
Analysis report. For most cases, in which a single part or component is being analyzed,
this outline will correspond to the general work flow. For those reports that present stress
analyses for widely different locations, and using different analysis techniques, it may be
more appropriate to repeat Sections 3 through 7 for each analysis.
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TABLE OF CONTENTS (TYPICAL)
REFERENCES
LIST OF ABBREVIATIONS AND SYMBOLS
LIST OF FIGURES
LIST OF TABLES
1.0 INTRODUCTION
Locations Analyzed
Certification Requirements
2.0 SUMMARY OF MARGINS
3.0 PART DESCRIPTION
4.0 LOADS
Load Development
Critical Load Cases
Critical Loads
5.0 MATERIAL PROPERTIES
6.0 ANALYSIS METHODS
7.0 STRESS ANALYSIS
1.0 INTRODUCTION
The introduction should include a brief summary of what the part is, why it is being
analyzed, what area of the part is analyzed, and what the final results are (is the part
substantiated?). The minimum margins of safety should be presented.
1.1 Locations Analyzed
Include a summary of each of the locations analyzed along with a brief description of
each one. Section 3 will present further details of the part.
1.2 Requirements
If the part is to be certified to particular strength regulations, then the applicable
paragraph numbers shall be listed. If additional requirements are being met, including
Cessna requirements, then those shall be listed also.
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2.0 SUMMARY OF MARGINS
A summary (usually in the form of a table) of each analyzed location and its margin of
safety. When appropriate, the nature of the failure should also be present—shear tear out,
crippling, inter–rivet buckling, etc.
3.0 PART DESCRIPTION
A description of the structure or parts analyzed will be given here. Sufficient figures
should be included in order to avoid any confusion of part location or orientation.
4.0 LOADS
A listing of the analyzed loads cases is given here. At its simplest, a singe load value or
G load may be sufficient. For others, a full accounting of shear, moments, and torques
will be needed. In any case, the loads used must be fully referenced and it must be clear
if any additional factors (such as 1.5) have been included. The loads development
process must be fully described. In most cases the applied loads will be supplied by
Cessna, in which case the full reference should be made.
5.0 MATERIAL PROPERTIES
A complete listing of the relevant material properties used in the analysis along with their
source is required here. A typical list might include:
Fty yield strength
Ftu ultimate strength
E Elastic Modules
n Ramberg–Osgood Number
Beyond these basic material properties, allowables for rivets, bolts, cables, bonds, etc.
would also be appropriate here.
6.0 ANALYSIS METHODS
This section will contain an overview of the analysis methods, assumptions, and tools
used. Primarily this involves the technique used to take the external, applied loads and to
calculate internal stresses or loads. The structure may be assumed to be linearly elastic,
with small deflections, or the non linear, elastic and plastic deflections may all be
accounted for. In many cases, a finite element model will be used. For these cases, a
description of the extent of the model along with a general discussion of the assumptions
made in its construction should be included. Depending on the model size, it may be
appropriate to include the full model definition in an appendix.
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7.0 STRESS ANALYSIS
This section will contain the actual analysis for each part or location. Each analysis
should:
1. Identify the specific load case used.
2. Explain why this location was selected (nature of criticality).
3. List any specific assumptions made (it may not be necessary to state the assumption
that plane regions remain plane, but if fasteners are assumed to carry loads
proportional to their capabilities, for instance, then that should be noted).
4. Identify the mode of failure (crippling, shear failure, etc.).
5. Clearly identify the final margin of safety.
6. Ensure the clear use of such terms as “ultimate”, “limit”, “factored”, etc.
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