PHARMACEUTICAL QUALITY
The FDA Center for Drug Evaluation and Research (CDER) Office of Pharmaceutical Quality’s (OPQ) 2017 Annual Report provides a panoramic snapshot of the Pharmaceutical Industry and the regulatory and quality activities therein. Established in 2015, the OPQ consists of over 1,300 staff responsible for regulating the quality of human drugs marketed in the US, providing assessment, inspection, research, surveillance, and policy for product quality, facilities and manufacturing processes.