Expert Consulting to the Life Sciences Industries
Aquity Associates comprises the primary categories of pharmaceutical expertise required to complete a Common Technical Document (CTD): Chemistry, Manufacturing, and Controls (CMC); Nonclinical Development, Pharmacology, and Toxicology; Clinical and Protocol Development, and Regulatory Science. Drs. Johnston, Bier, Gorelick, and Scalfarotto offer an integrated approach to handle your consulting needs for drugs, biotech products, and medical devices, from bench to regulatory approval.