Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries 2014 is a webinar that covers topics such as:
- 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
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries 2014 is intended for:
- Quality System Auditors
- Quality & Regulatory Professionals
- Marketing Product Managers
- Manufacturing & Design Engineers
