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Suzette Mctigue Roan

Suzette Mctigue Roan MS, JD

Senior Director | Cambridge, Massachusetts    United States of America
Pharmacy And Medicine, Mental Health And Law
Mental Health And Law, Pharmacy And Medicine,...More
Spoken at 4 events

Biography :

Suzette joined Biogen’s Regulatory Affairs CMC group in 2014, focusing on combination product and devices. Prior to Biogen, Suzette was with Pfizer from 1995 until 2014, with roles in Analytical, Outsourcing and Regulatory CMC. She has experience with pulmonary inhaler, prefilled syringe and autoinjector delivery systems. Suzette holds a BS in Chemistry from the University of Connecticut, a MS in Management from Albertus Magnus College and a JD from the University of Connecticut School of Law. Previously, Suzette was the Co-chair of the IPAC-RS Supplier QC Working Group, served on the IPAC-RS Board of Directors and helped develop PS 9000:2011, Guideline for Pharmaceutical Packaging. She is currently a member of the Combination Products Coalition, AAMI and ISO committees.

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Pharmacy and Medicine, Mental Health and Law

Interested Topics

Mental Health and Law, Pharmacy and Medicine, Biopharmaceuticals, Drug Development, Medical Devices, Chromatography, Regulatory Requirements, Validation, Quality by Design, Polymer Characterization, Device Regulatory

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MOC / CME / CE Requirements
Virginia Board of Medicine

Virginia Board of Medicine accepts the courses that are endorsed by ACCME and grants AMA PRA Category 1 credit.

MD/DO Requirement:

CME Credits Required : 60.00 | Licensing Cycle AMA PRA : 2 Years | Category Credits : 30.00



  • 60 hours of CME for every 2 years followed by immediate preceding renewal
  • A minimum of 30 hours must be under Category 1, of which 2 hours must be in pain management, proper prescribing of controlled substances, and the diagnosis of management of addiction.
  • OCC/MOC is not specifically addressed, but an endorsement of recertification by a specialty board is admitted as a substitute by the Virginia Board of Medicine.