The medical device industry is buzzing with information about ISO 13485:2016.
The final deadline for compliance is
February 28, 2019, but a transition plan and registration audits take time.
Pilgrim is here to help you every step of the way. As you work through the gap analysis phase or the transition, you’ll need to closely examine many processes, especially your quality management processes.
In this e-book, we’ll focus on specific quality management processes and take a closer look at how you can build risk-based thinking into each of them in accordance with the latest version of the standards.
Download this e-book to learn more. »