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Mario Mendoza, MD, MS

New York State Center for Biotechnology at Stony Brook University
Dr. Mario R Mendoza is a clinical anesthesiologist (practiced at the NIH), chemist, and currently an independent healthcare and pharma medical affairs consultant with over 13 years of combined experience in patient care, clinical development, R&D, medical affairs (Abbott, Pfizer and Centrexion Therapeutics), and FDA medical devices regulation.
Dr. Mendoza’s expertise is within therapeutic area agnostic medical/patient care and medical devices medical/regulatory consulting; as well as medical affairs strategy, tactics within all pillars (inclusive of KOL engagement, commercial collaborative work, unbranded/branded medical content development, publications strategy and compliance, IIR/IIS, Phase 4/Pharmacoeconomic studies). He also has additional expertise within the acute/chronic pain, opioid abuse, and cardiovascular therapeutic areas.
Dr. Mendoza earned his BS degree in chemistry from SUNY College at Old Westbury, and an MS in organic chemistry from the University of Illinois at Urbana-Champaign. He earned his M.D. from the University of Illinois at Chicago College of Medicine and then completed an FDA Commissioner’s Fellowship Program and stayed on at FDA, as a Medical Officer/Medical Consultant.