Date: 13-14 July 2017
Location: Alexandria, Virginia
Mindy McCann, Vice President Regulatory Affairs at Qserve is invited as a speaker at the Q1 European Medical Device Regulation Conference in Alexandria. She will be giving a workshop on “Impact Assessment – Identifying necessary Regulatory Revisions”: Determining EU MDR compliance gaps in corporate regulatory structure Risk-based approach to new rules & the regulatory strategy revision Engaging with other teams to ensure all areas of impact are addressed Implementing a thorough & detailed regulatory revision plan.
Q1 has over a dozen years of experience in providing high-level educational content for the European Medical Device Industry and is consistently ranked by participants as delivering quality program content, speaker selection, and facilitation. This program is unique in that it is specifically for global companies based in the United States to understand the new regulatory rules in Europe. All content is delivered by medical device industry experts, and notified bodies as keynote panels, case studies, fireside chats, workshops, and master classes so you will return to the office with tangible ideas that may be implemented immediately.
The agenda of this event can be downloaded here.
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