Elements of a CAPA System and Uses of CAPA Data - 2017
WebcastFaculty
OVERVIEW
Elements of a CAPA System and Uses of CAPA Data is organized by Compliance4All and would be held on Jun 19, 2017.
Overview:
Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer.
Areas Covered in the Session:
• Regulatory Requirements
- FDA QSR
- ISO 13485
• Elements of a cross-procedural CAPA program
• Applications of CAPA
• CAPA Data, and best practices for its use
• Application of risk management to CAPA program
Overview:
Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer.
Areas Covered in the Session:
• Regulatory Requirements
- FDA QSR
- ISO 13485
• Elements of a cross-procedural CAPA program
• Applications of CAPA
• CAPA Data, and best practices for its use
• Application of risk management to CAPA program
SPECIALITIES
Medical EducationHealth Informatics
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