ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2014 is a webinar that covers topics such as:
- How ISO 1497:2012 differs from ISO 14971:2007
- What is ISO 14971
- How to make sure your Risk Management procedure assures you can meet your CE mark requirements for Risk Analysis
- How to update your Risk Analysis to meet continued compliance to the European Medical Device Directive(MDD)
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2014 is intended for:
- Regulatory Affairs
- Quality Management
- Design Engineers
- Quality Engineers
- Quality auditors
- Compliance managers