Dunne and Moore Train FDA Staff on Drug Manufacturing Laws

Silver Spring, Maryland
Shook, Hardy & Bacon Partner Debra S. Dunne, R.Ph., and Senior Associate Tim Moore provided in-house training to staff at the FDA’s Center for Drug Evaluation and Research’s Office of Pharmaceutical Quality on Nov. 23, 2015, at the FDA’s White Oak Campus in Silver Spring, Maryland. The pair were invited to participate in the Food and Drug Law Institute’s Introduction to Drug Law and Regulation, which is specific to the Food and Drug Administration. Dunne and Moore’s presentation covered the ways that the government regulates drug manufacturing, including establishment registration, drug listing, adulteration, current good manufacturing practices (cGMP) regulations, and FDA inspections.