How FDA Trains its Investigators to Review CAPA and What you Should do to Prepare
Instructor: Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Year after year, CAPA is the subsystem cited most frequently during FDA inspections. During an inspection, FDA personnel will take a great deal of time reviewing your company's CAPA system. What will they look for? This session will discuss techniques used by the FDA to review your CAPA system. The documents used by FDA to train their inspectors to review your CAPA system will be explained, some of which you may not be familiar with.
Also contained in this session will be a section-by-section summary of the CAPA subsection of the QSIT, the document by which FDA inspectors operate during an inspection, as well as how your company can use that same document to increase the likelihood of a positive outcome during the inspection.
Areas Covered in the Session:
- Documents Used by FDA Inspectors
- Investigations Operations Manual (IOM)
- CAPA Implications
- Recommended Methods of Compliance for each Requirement
- CPG Manual 7382.845
- CAPA Implications
- Recommended Methods of Compliance for each Requirement
- QSIT Manual
- Description of each CAPA Inspectional Objective
- Recommended Methods of Compliance
Who Will Benefit:
- QA Management
- CAPA Coordinator
- Regulatory Affairs Management
- Executive Management
- Consultants
- Quality System Auditors