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Regulatory Requirements for Pharmaceutical Products

A required course in the Certificate Program Clinical Trials: Medical Device and Drug Development.

Course closed to new registrations: Call ( 949 ) 824-5414 for more information or sign up below to be notified when this course becomes available.×

Course Description

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.

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  • Details
  • $735
  • June 21, 2021 to August 29, 2021
  • Delivery Mode: Online
  • Reg#: 00173
  • ID/Units: EECS X445.26  (3.00)
    ( Section 1 )
  • Quarter: SUMMER 2021

Instructor


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.

Textbook Information

Textbooks for your course may be purchased from any vendor or bookseller of your choice.

Required Textbook(s):

A PRACTICAL GUIDE TO FDA'S FOOD AND DRUG LAW AND REGULATION
Book - ISBN: 9781935065876
Kenneth R. Pina & Wayne L. Pin, 7 ed, The Food and Drug Law Institute

Meeting Schedule

EventDateDayStart TimeEnd TimeLocationRoom
START06/21/2021Monday------Online (Access Begins)---
END08/29/2021Sunday------Online (Access Ends)---