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 meet compliance standards ahead of their competition.
In this webinar — specifically designed for product and engineering teams building medical devices — you’ll learn how to move beyond the frustrations of document-based requirement systems and the added overhead of regulatory requirements to streamline your development and set yourself apart from the competition. Our experts will cover how you can:
- Bring systems thinking into design control activities using Jama Connect
- Align how you work with the development of the artifacts needed for compliance and the Design History File (DHF)
- Develop products through the lens of traceability
- Use Jama Connect to align your development process with relevant parts of governing regulations ISO 13485:2016 & 21 CFR 820.30
