How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare 2018 is a webinar that covers topics such as:
- CAPA Implications of Investigations Operations Manual (IOM), and Recommended Methods of Compliance for each Requirement
- Documents Used by FDA Inspectors
- QSIT Manual: Description of each CAPA Inspectional Objective, and Recommended Methods of Compliance
- CAPA Implications of CPG Manual 7382.845, and Recommended Methods of Compliance for each Requirement
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare 2018 intended for:
- CAPA coordinators
- Quality Departments
- Executive Management
- Regulatory Affairs Departments
- Quality System Auditors
- Consultants
