Drew Barlow, MPH

Syner-G Pharma Consulting

Vice President, Regulatory Affairs

Drew Barlow is Vice President, Regulatory Affairs at Syner-G Pharma Consulting, where he oversees the firm’s regulatory function. Syner-G consists of three core business units (Regulatory, CMC Development, and cGMP Compliance) and helps to design and implement science and risk-based, phase-appropriate CMC (chemistry, manufacturing and controls) solutions.

Before joining Syner-G in 2014, he held positions in regulatory CMC at Alkermes and Vertex Pharmaceuticals. Prior to Vertex, he served as an Investigator with the US FDA’s Office of Regulatory Affairs, specializing in GMP compliance.

Mr. Barlow's areas of expertise include devising CMC strategies for phase-appropriate regulatory filings, marketing application preparation, and GMP readiness.

He holds a B.S. in biology from Mount St. Mary’s and Master of Public Health (MPH) from University of North Carolina at Greensboro.