study close out
DESCRIPTION
STUDY CLOSE OUT. Definition. This relates to the closure of a study at a participating site once all subjects have completed the study and all data queries have been resolved. Note:. Close out is not a one-off visit but is a process that may take weeks to months to complete - PowerPoint PPT PresentationTRANSCRIPT
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STUDY CLOSE OUT
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Definition
• This relates to the closure of a study at a participating site once all subjects have completed the study and all data queries have been resolved.
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Note:
• Close out is not a one-off visit but is a process that may take weeks to months to complete
• Can have multiple close out visits• It is essential that data and information are
retrievable and stored in a safe and logical manner. This process must be conducted in accordance with GCP and regulatory requirements.
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Key areas
Use the study close out SOP to provide guidance but the key areas are as follows:– Study documentation– Data Management– IRB/RA– Drug Accountability– Sample storage
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Study Documentation
• Study filing: Ensure filing of documentation has been maintained throughout the study and provides a clear audit trail
• Archiving: Meet archiving requirements and make corresponding arrangements
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Data Management
• Data Validation: Completed data entry and all queries are resolved.
• Electronic Data: mainly sponsor responsibility• Serious Adverse Event (SAE) Reconciliation
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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IRB/RA
• Inform IRB, RA (if applicable) and local institution.
• The reason for premature termination of a site if study stopped early.
• All relevant safety issues and safety updates at and after close-out
• The date of site closure
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Drug Accountability
• Reconcile accountability, supply and inventory logs for the study product.
• Ensure proper documentation for return of product or drug destruction.
• Any deviations should be documented.
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Sample storage
• Ensure long-term storage of clinical samples meets the requirements and is documented
e.g. storage of baseline(screening) malaria slides or exportation of pk samples
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008
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Closing remarks
• The study should be closed out such that its ready for an audit or inspection at a later date, as late as 10 years from now!
KEMRI-Wellcome Trust Research Programme Version: 4-Nov-2008