Choosing the Right Solution for ISO 13485:2016 Compliance

Preparing for ISO 13485:2016 poses challenges to medical device manufacturers throughout the world.

The revised standard has significant updates in the areas of risk-based quality processes and supplier management, as well as an increased focus on ensuring regulatory compliance throughout the quality system.

Pilgrim has enhanced our already-robust compliance with ISO 13485:2016 with these areas in mind to keep your business on track for a successful transition.

Join us for this live webinar to learn:

• What are the key changes within ISO 13485:2016 and how will they affect your quality system?
• How does an automated quality management system (QMS) simplify ISO 13485 compliance?
• Which specific SmartSolve^® solutions will support your compliance efforts?

Register now to get the tools you need to keep your ISO 13485:2016 transition moving forward smoothly.

Can't make it? Register anyway, and we'll send you the on-demand recording. »