MCRA
Mehdi Kazemzadeh-Narbat, PhD, PMP, serves as the Director at MCRA, an IQVIA business, where responsibilities include developing regulatory services for medical device submissions and managing business development functions. With extensive experience in regulatory strategy and compliance, Mehdi has held positions at the FDA, focusing on orthopedic and dental devices, and previously worked in R&D roles, supervising teams and developing innovative biomedical products. Educational background includes a PhD in Biomedical Engineering from The University of British Columbia, highlighting a strong foundation in biomaterials and medical device evaluation.
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MCRA
MCRA is a leading advisory firm and Clinical Research Organization (CRO) to medical technology developers. Core areas of expertise include regulatory, reimbursement, clinical research, healthcare compliance and quality assurance.