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Introduction to Risk Management for Medical Devices

When building complex, safety-critical products, risk management is essential. But compliance standards — such as ISO 14971 and TIR36:2007 — can be tricky to navigate.

A risk management process helps determine validation requirements and ensures safety is designed into a medical device product and related software.

Join us to:

  1. Get clarity on the standards for medical device hardware and software development
  2. Learn what you need to stay compliant
  3. Find out how to prove you took the necessary steps to achieve compliance
Kelly Weyrauch Founder Agility Quality Systems
Cary Bryczek Principal Solutions Architect Jama Software
 
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