Move from Document-Based Design Control and Risk Management: Improve Collaboration, Quality and Delivery in Medical Device Development

Medical device companies are on the cutting-edge of advancing health care. Along with facing relentless pressures to innovate and release quality products, they also must comply with regulations and standards to remain competitive.

In this webinar, specifically designed for product and engineering teams building medical devices, you’ll learn how to move beyond the frustrations of disconnected, document-based requirement systems, streamlining your design and development and risk management processes while maintaining compliance with applicable regulations and standards.