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.