How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

Overview:

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 all the documents used by FDA to train their inspectors to review your CAPA system, 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 in your preparation. 

Areas Covered in the Session:

• Documents Used by FDA Inspectors
• CAPA Implications of Investigations Operations Manual (IOM), and Recommended Methods of Compliance for each Requirement
• CAPA Implications of CPG Manual 7382.845, and Recommended Methods of Compliance for each Requirement
• QSIT Manual: Description of each CAPA Inspectional Objective, and Recommended Methods of Compliance

Who Will Benefit: 

This webinar will provide valuable assistance to all regulated companies, since a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:

• R&D Management
• Regulatory Management 
• QA Management 
• Consultants 
• Quality System Auditors

Quick Contact:

GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com
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