Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015
27 Aug 2015
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 nonconformities
Examples of Containment actions
Where does Preventive Action fit in
Who should Attend
QA Specialists
Quality Managers
Quality Engineers
CAPA coordinators
Operations managers
Engineers doing Corrective Actions
Quality auditors
Manufacturing Engineers
Medical device Consultants
Past Events
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015 - 27 Aug 2015, Webinar (52644)
Important
Please, check "Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Quality assurance
Education: E-learning, Training
Government & Global Issues: Law & Regulations
Health & Medicine: Medical laboratories, Medical technology
