When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation 2013 is a webinar that covers topics such as:
- Why Containment and Correction have been overlooked
- Overview of CAPA system for Current ISO 13485 compliance
- What is really the difference between correction and corrective action
- Why this is a hot item with ISO auditors
- Defining and documenting Containment actions - Quickly
- What kinds of containment can be done for Quality System non-conformities
- Examples of Containment actions
- Where does Preventive Action fit in
When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation 2013 brings together:
- Medical Device CAPA coordinators
- Medical Device Quality Management
- Medical Device Engineers doing Corrective Actions
- Medical Device Quality Engineers
- Medical Device Manufacturing Engineers
- Medical Device Operations managers
- Medical Device Quality auditors
