Balancing Compliance & Innovation in the Medical Device Industry

Wednesday, February 20, 10:30 a.m. PT

Medical device companies are rapidly advancing health care. Along with feeling relentless pressures to innovate, 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:

  1. Bring systems thinking into design control activities using Jama Connect
  2. Align how you work with the development of the artifacts needed for compliance and the Design History File (DHF)
  3. Develop products through the lens of traceability
  4. Use Jama Connect to align your development process with relevant parts of governing regulations ISO 13485:2016 & 21 CFR 820.30

Zeb Geary

Sr. Consultant,
Jama Software

Zeb has more than a decade of experience in software consulting, including multiple years working with a wide variety of medical device companies. In addition to serving as the architect of Jama’s Medical Device Services, Zeb has also helped many of Jama’s enterprise customers deploy and optimize their use of the Jama Product Development Platform.