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Subscribe NewsletterA CAPA Primer - Elements of a CAPA Program and Uses of CAPA Data
Product Id
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600062
Overview: A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer.
A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings. This session will discuss the importance, requirements, and elements of a CAPA program, as well as describing the uses of CAPA data. Additionally, the application of risk management to a CAPA program will be reviewed, and a specific risk management system explained.
A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings. This session will discuss the importance, requirements, and elements of a CAPA program, as well as describing the uses of CAPA data. Additionally, the application of risk management to a CAPA program will be reviewed, and a specific risk management system explained.
Areas Covered in the Session:
- QSR and ISO 13485 requirements for CAPA
- Elements of a cross-procedural CAPA program
- Applications of CAPA
- CAPA data and its uses Application of risk management to CAPA program
Who Will Benefit:
- Regulatory Management
- Quality Assurance Professionals
- Consultants
- Sales/Marketing Management
- Senior and mid-level Management
- Quality System Auditors