On-Demand Webinar
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.
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