ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2019
02 Apr 2019
Webinar
Description
Topics
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
Who should Attend
Medical Device Regulatory Affairs
Medical Device Quality Management
Medical Device Design Engineers
Medical Device Quality Engineers
Quality auditors in medical device companies
Compliance managers
Past Events
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2019 - 02 Apr 2019, Webinar (54155)
Important
Please, check "ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements" official website for possible changes, before making any traveling arrangements
