Marcia Arentz

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Medical Device Submissions 5502

Medical Device Compliance 5496

Ms Arentz has over 25 years of experience in quality assurance and regulatory affairs with medical device companies including in vitro diagnostic devices, orthopaedic implant devices and pharmaceutical delivery systems. During her career, she has authored over 60 FDA submissions and has published articles in RAPS Focus Magazine. She has a B.S. in Chemistry, an MBA, and completed her Temple University MS-QA/RA in 2002. She holds professional certification as an ASQ Certified Quality Auditor and has her RAC from the Regulatory Affairs Professional Society.

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