Christopher Snyder, MS
Chris provides regulatory; chemistry, manufacturing, and controls (CMC); and compliance support to the pharmaceutical products industry. He is experienced with authoring and reviewing CMC sections of Investigational New Drug Applications (INDs), Investigational Medicinal Product Dossiers (IMPDs), and New Drug Applications (NDAs), as well as Standard Operating Procedures (SOPs). Additionally, he provides cGMP auditing and CMC quality oversight support. Additionally, Chris provides regulatory operations support and has experience coordinating, drafting, formatting, publishing, and transferring electronic submissions for filing to the U.S. Food and Drug Administration (FDA). Chris has a B.S. in Biology from Stevenson University and an M.S. in Biotechnology, with a Concentration in Regulatory Affairs from Johns Hopkins University.