Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015 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 nonconformities
Examples of Containment actions
Where does Preventive Action fit in
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors 2015 is intended for:
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