Hear from Industry Experts in the U.S., Europe, and Japan on key regulatory and clinical trends around the world

• James Mullally, Ph.D., Vice President, IVD Regulatory Affairs, US, MCRA
Former FDA Assistant Director, Chemistry and Toxicology Devices Division

• Erica Conway, Ph.D., Vice President, IVD Regulatory Affairs, Europe, MCRA
Former Head of Notified Body - IVD at BSI

• Samuel Pollard, General Manager, Vorpal Technologies, K.K. (a MCRA subsidiary)
10+ years leading global regulatory submissions

• Julie Martel, Ph.D., Vice President, IVD Clinical Affairs, MCRA
25+ years IVD Clinical Experience

MCRA is the leading industry-specialized CRO and integrated advisory firm that assists clients through the entire technology life cycle, from strategic planning through commercialization.

#medtech #medicaltechnology #ivd #invitrodiagnostics

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