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2020 - ISO 14971:2019 – What’s new in the updated standard?
Date2020-05-27
Deadline2020-05-17
VenueOnline Event, USA - United States 
KeywordsISO 14971:2012 compliance; Medical Device Risk Analysis; CE Mark requirements
Topics/Call fo Papers
How ISO 1497:2019 differs from ISO 14971:2012
How to update your Risk Analysis to meet continued compliance to the European Medical Device Directive(MDD)
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)
How to make sure your Risk Management procedure assures you can meet your CE mark requirements for Risk Analysis
Other CFPs
- Risk-Based Software V&V Per U.S. FDA, IEC 62304, GAMP 5 (Reg.) and ISO 14971
- FDA and MHRA Guidance during the COVID-19 Emergency: Medical Devices and Diagnostic Tests
- Medical Device Industry Trends for Computer Systems Regulated by FDA
- Understanding Key Quality System Requirements for Combination Product (Medical device and Pharmaceuticals) Manufacturers
- FDA Inspection Readiness
Last modified: 2020-05-07 00:39:42