FDA MedTech Regulatory Forum – EU MDR Panel

Catch R&Q in Akron, OH on August 22, where Nancy Morrison will be pulling double duty, moderating and presenting, on EU MDR.

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August 22, 2019 — Akron, OH

Moderating and presenting? Nobody who knows R&Q's Executive Director of Regulatory & Quality Consulting Services, Nancy Morrison, is surprised. Nancy will be pulling double duty during for an EU MDR transition session at BioOhio's FDA MedTech Regulatory Forum on Thursday, August 22nd.

Read on for all the details.





EU MDR Transition Progress (panel discussion)





Bounce Innovation Hub

526 S. Main St.

Akron, Ohio 44311





Thursday, August 22nd: 1:15pm





Holly Lee – Senior Manager, Post-Market Surveillance
Philips Medical


Notified Body (still to be announced)

Nancy Morrison – Executive Director, Regulatory & Quality Consulting Services
Regulatory & Quality Solutions (R&Q)

Nancy_Morrison_1-min-429968-edited.jpgNancy has over 25 years of quality and regulatory experience in the medical industry with US and global regulatory submission experience. The previous five years have been with R&Q working with start-up, mid-size and multi-national medical device and combination product companies. Nancy has a Bachelor of Science in Mathematics and an Advanced Certificate in Regulatory Affairs along with RAC certifications for the US and EU. Nancy has the ability to build collaborative relationships with stakeholders to utilize regulations to identify opportunities that provide compliant and effective business solutions.

Check out all the event details and register here.