The medical device industry faces heavy regulations, and for good reason. With lives at stake, patient safety is of the highest importance.
Failure to adhere to FDA, EU, and other standards and regulations leads to embarrassing and costly product recalls. The case for quality and compliance is critical. Your profits, and indeed your company, are on the line.
Listen to Sri Tupil, Vice President of Software Quality Engineering and Product Management at Fresenius and Michelle Boucher, Vice President for Research at Tech-Clarity discuss current industry trends. The webcast will also cover:
- The Case for Quality and how manufacturers can bridge current gaps.
- How manufacturers should respond to rigid FDA or EU regulations and authorities.
- Fresenius´ approach to the case for quality and how they apply current trends in practice.
- Questions & Answers session.