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?
View this 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.

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.

Download this on-demand webinar to learn more. >>

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