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:
- Get clarity on the standards for medical device hardware and software development
- Learn what you need to stay compliant
- Find out how to prove you took the necessary steps to achieve compliance