Recent amendments to the European Union Medical Device Regulation (MDR) have left many developers questioning how to stay compliant while remaining efficient and innovative. By carefully integrating risk management into preclinical animal studies, you’ll gain an advantage over competitors by being able to proactively anticipate any risks that could prevent your medical device from reaching the market.
In this webinar, you’ll learn how to:
- Implement integrated risk management for the development of new medical devices
- Design appropriate preclinical studies to mitigate any remaining preclinical risks
- Predict clinical risks to ensure your device is MDR-compliant before it reaches the market
Michaela Hajek PhD, MBA
Louis-Georges Guy, PhD, DESS G
Senior Director of Science
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