ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2019 is a webinar that covers topics such as:
- How to update your Risk Analysis to meet continued compliance to the European Medical Device Directive(MDD)
- How ISO 1497:2012 differs from ISO 14971:2007
- How to make sure your Risk Management procedure assures you can meet your CE mark requirements for Risk Analysis
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2019 is intended for:
- Medical Device Regulatory Affairs
- Medical Device Quality Management
- Medical Device Design Engineers
- Medical Device Quality Engineers
- Quality auditors in medical device companies
- Compliance managers
