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Thursday, April 13, 2017
11:00 a.m. EST

shutterstock_349750148.jpgThe deadline for ISO 13485:2016 compliance is getting closer every day. Most affected medical device manufacturers have begun a gap analysis and started planning for the transition. Now it’s time to take the next step.

Are you ready to move forward?
Join us for this upcoming webinar to dig deeper into the changes and challenges being faced by industry leaders as they begin their transition. During the presentation, Dan O’Leary, President of OMBU Enterprises, will present specific processes and areas that will need attention as you’re filling in the compliance gaps within your own organization.

Register Now

This webinar will help you:

  • Understand the timing and overlap between ISO 13486:2016 requirements and other emerging global regulations.
  • Explore quality processes that need additional attention for a proper transition, especially supplier controls and customer complaints.
  • Review the many ways that risk and risk management will impact your quality system.
  • Define areas where QA personnel will need to increase regulatory focus in their day-to-day activities.

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

This webinar is the second of a 4-part quarterly series devoted to ISO 13485:2016 compliance. Register today to save your seat.

Can't Make It?
Register anyway and we'll send you the recording on-demand.