A required course in the Certificate Programs in Medical Product Development, and Clinical Trials: Medical Device and Drug Development; and a prerequisite in the Specialized Studies Program in Regulatory Affairs Management.
This course presents a detailed overview of the regulatory requirements for the discovery, development, and commercialization of pharmaceutical products (drugs and biologics). Individuals involved in manufacturing, quality control, research and development, and clinical studies will learn the latest information. Explore topics that include the product development process through commercialization, product characterization and pre-clinical evaluation, pharmaceutical industry requirements, clinical trial requirements, good manufacturing practices (GMPs), good laboratory practices (GLPs) and inspections, labeling medical products and writing Food and Drug Administration (FDA) submissions.
Erin Messer, PharmD, MBA serves as a Faculty Program Advisor for Independence University school of Healthcare – Allied Health, and an adjunct instructor for the United Career Institute. She has over 10 years of experience working in the pharmaceutical industry, including drug formulation, development and regulatory submission.
Textbooks for your course may be purchased from any vendor or bookseller of your choice.
A PRACTICAL GUIDE TO FDA'S FOOD AND DRUG LAW AND REGULATION
Book - ISBN: 9781935065708
Kenneth R. Pina & Wayne L. Pin, 5 ed, The Food and Drug Law Institute
|Event||Date||Day||Start Time||End Time||Location||Room
|START||06/21/2021||Monday||---||---||Online (Access Begins)||---
|END||08/29/2021||Sunday||---||---||Online (Access Ends)||---