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starting-line-1-1.jpgThe 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. 

Get in the Race: Perform a Gap Analysis
In this on-demand webinar, Dan O'Leary, President of OMBU Enterprises, presents his insights on how to approach an ISO 13485:2016 gap analysis, and discusses specific areas on which you should focus during the transition.

Learn Additional Industry Insights
Plus, Pilgrim's in-house Regulatory Analyst, Deb Kacera, will present details on how members of Pilgrim's Regulatory Advisory Board are preparing for the transition, including specific areas where they've faced challenges. 

You'll leave the webinar with actions you can immediately leverage to get started or proceed with your ISO 13485:2016 gap analysis and transition plan. 

Support for Every Step of the ISO 13485:2016 Transition
With the onset of MDSAP, timely ISO 13485 compliance is becoming more critical than ever before. Pilgrim is here to help you every step of the way.

This webinar is the first of a 4-part series devoted to ISO 13485:2016 compliance. 

Watch the on-demand webinar to learn more. »



     

 

 

 

 

 

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