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iso-with-two-doors.jpgPreparing 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.

Download this on-demand 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?

Download this on-demand webinar to learn more. »

Register Now!