Recorded November 10, 2022 | On-Demand Webinar
Learn Current Good Manufacturing Practices (cGMPs) for drugs and be able to define “adulteration” and “misbranding”. Understand the different types of inspections, including the differences between foreign and domestic inspections. Recognize the elements of a 483 observation and the components involved in closing out an inspection.
This session was recorded as part of FDLI’s virtual Introduction to Drug Law and Regulation course in November 2022.