Sr. Director, Reg. Affairs
Quidel
Frank Pokrop has worked in the drug and medical device industries for more than 20 years and has obtained these certifications: CSQE, CISA, CPGP and RAC. Frank is a senior director of regulatory affairs at Quidel in San Diego where he leads the implementation of the IVDR regulation and manages post market functions.
His background includes worldwide submissions and product approvals, recall management, leading global compliance and auditing programs, product launches, vigilance reporting, and he has worked in manufacturing for both drugs and devices. He was a member of the Editorial Advisory Board for MDDI magazine from 2006 – 2016.
At UC San Diego he has: (1) Taught courses on medical device submissions, and, (2) Served on the IRB for 4 years.
He is a member of the Board of Directors for RAPS. He is currently a member of the FDA Committee on Hematology products. He volunteered at the San Diego Regulatory Affairs Network (SDRAN) for 10 years serving as President and VP of programs and he lives in Carlsbad with his wife and a female chocolate Labrador.
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Tuesday, September 13, 2022
3:30 PM – 4:30 PM MST