When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation 2013
04 Apr 2013
Webinar
Description
Topics
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
Who should Attend
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
Past Events
When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation 2013 - 04 Apr 2013, Webinar (37590)
Important
Please, check "When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical technology
