Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries 2014
04 Mar 2014
Webinar
Description
Topics
ISO 9001 & ISO 13485 Differences
Principles of ISO 13485:2003
FDA’s MDR’s & EU Vigilance
Risk Management & ISO 14971
MDD 93/42/EEC & Essential Requirements
Design Control
Who should Attend
Quality System Auditors
Quality & Regulatory Professionals
Marketing Product Managers
Manufacturing & Design Engineers
Past Events
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries 2014 - 04 Mar 2014, Webinar (14907)
Important
Please, check "Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries" official website for possible changes, before making any traveling arrangements
