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Updated CE Marking Process & ISO 13485:2016 Expectations 

When: Fri., July 12, 10-11:30 a.m. 2019
Phone: 800-447-9407
Email: compliance4all14@gmail.com
Price: $ 150.00
www.compliance4all.com
Overview: This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU. It includes specific insights from direct involvement and work within the EU and the Commission's major improvement objectives to their system today.
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