FMEA and Risk Management for Medical Devices 2012

20 Sep 2012

Webinar

Key Topics

Risk Management vs.ISO 13485:2003
FMEA & FMECA
FDA`s Risk Management Requirements
Risk Management & ISO 14971
Medical Device Directives & Risk Management
Design Control Risk Management

Who should Attend

Quality System Auditors, Quality & Regulatory Professionals, Marketing Product Managers and Manufacturing & Design Engineers.

Past Events

FMEA and Risk Management for Medical Devices 2012 - 20 Sep 2012, Webinar (32792)

FMEA and Risk Management for Medical Devices 2026

Important

Please, check "FMEA and Risk Management for Medical Devices" official website for possible changes, before making any traveling arrangements

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Government & Global Issues: Law & Regulations

Health & Medicine: Healthcare, Medical laboratories, Medical technology, Pharma

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