the dynamic environment of laws, regulations and policy
DESCRIPTION
The Dynamic Environment of Laws, Regulations and Policy. Coming to Grips with uncertainty in the process. Richard M. Lewis, PhD Access BIO, LC [email protected]. Or:. What are they thinking? What do they really want? What did they mean by that?. Federal Register. - PowerPoint PPT PresentationTRANSCRIPT
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The Dynamic Environment of Laws, Regulations and Policy.Coming to Grips with uncertainty in the process
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Or:
What are they thinking?
What do they really want?
What did they mean by that?
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Federal Register
Official Government PublicationDaily
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Federal RegisterExecutive Orders and ProclamationsRules and RegulationsProposed RulesNotices
Availability of GuidancePublic meetings
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The Laws
Order of EnactmentStatute - Congress and ExecutiveRegulations - Executive Agency, FDAGuidance - Agency, CenterSOP - Center
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Example: Statute
Food and Drug Administration Modernization Act of 1997To amend the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act to improve the regulation of food, drugs, devices and biological products, and for other purposes, Nov. 21, 1997.
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Example Regulation21 Code of Federal Regulation
• PART 601 -- LICENSING• Subpart C--Biologics Licensing• Sec. 601.20 Biologics licenses; issuance and conditions.
• (a)Examination--compliance with requirements. A biologics license application shall be approved only upon examination of the product and upon a determination that the product complies with the standards established in the biologics license application and the requirements prescribed in the regulations in this chapter including but not limited to the good manufacturing practice requirements set forth in parts 210, 211, 600, 606, and 820 of this chapter.
• (b)Availability of product. No biologics license shall be issued unless:• (1) The product intended for introduction into interstate commerce is
available for examination, and• (2) Such product is available for inspection during all phases of
manufacture.• [64 FR 56451, Oct. 20, 1999, as amended at 70 FR 14983, Mar. 24, 2005]
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Example: Guidance• Guidance for Industry: For the
Submission of Chemistry, Manufacturing and Controls and Establishment Description Information for Human Plasma-Derived Biological Products, Animal Plasma or Serum-Derived Products February,1999.
• Guidance for Industry: For the Submission of Chemistry, Manufacturing and Control and Establishment Description Information for Human Plasma-Derived Biological Products or Animal Plasma or Serum-Derived Products“ January 21, 1998.
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• CBER SOPP, Sections 8400, Marketing
Applications• SOPP 8401: Administrative Processing of
Original Biologics License Applications (BLA) and New Drug Applications (NDA)Effective Date: April 25, 2013
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Comment Opportunity for comment for nearly all Regulations and Guidance
http://www.fda.gov/aboutfda/contactfda/commentonregulations/default.htm
Time Form
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What’s your product?Where is it regulated?Center and Office differences in policy.
Toxicology
Differences in GMPdrugs v biologics v devices
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Office of the Commissioner
Office of Combination Products
Center for Devices and Radiologic
Health
Center for Veterinary Medicine
Center for Biologics
Evaluation and
Research
Center for Food Safety
and Nutrition
Center for Biologics
Evaluation and
Reserach
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Public Meetings
Advisory CommitteesJoint IndustryJoint ScientificPart 15
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Advisory Committeeshttp://www.fda.gov/AdvisoryCommitteesThere are 50 different FDA advisory committees
Center specificOffice/Product specific
Open to the publicTranscripts Available from FDA (time lag)
Video available commercially.
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Public MeetingsPart 15 (21 CFR, Part 15)15.1. The Commissioner concludes, as a matter of discretion, that it is in the public interest to permit persons to present information and views at a public hearing on any matter pending before the Food and Drug Administration.The FDA has representatives who can ask clarifying questions.
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OrganizationsBIODIAPharmaRAPSFDLIAdvaMed
MDMASOTASCO
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Organizations
Annual meetingsJoint Workshops
FDA-BIO
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Meetings hosted with Industry or Scientific Community
• Usually on a specific issue• Industry Organizations
• BIO
• DIA
• Pharma
• NIH
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Services Distribution ListsBIO Smartbrief
DailyRAPS
DailyLinkedIn forums
FDA
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Specific Product Reviews
• Clinical• Pharmacology
• CMC• Toxicologic• Statistical• Summary Basis for Approval
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EMA Reviews
• EPAR: European Product Assessment Reports• Example: Humira, 243 pages
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Product Labels
• What is there• What is not there
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Meetings with the FDA
• Pre IND• IND• Pre Phase 3• Pre BLA
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Meetings• Type A: (within 30 days of request)
• Necessary for stalled development, e.g., IND on Hold
• Type B: (within 60 days of request)• PreIND, End of Phase 3/pre-phase 3, Pre-
BLA/NDA
• Type C: (within 75 days)All others.
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Enforcement
• 483s• warning letters• Untitled letters
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Consultants !
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