Medical Product Quality Systems – The Basics Learn more

- Are you a health care professional or related to the field of medicine in any capacity?
- Do you want to learn about the basics regarding the procedures and regulations involved in performing clinical trials of medications and treatments?
- Are you seeking an online course about this?
If this is the case then you have come to the right place. This package contains a course that has been designed to give you the basic tips and information about the process of drug development, trials and quality assurance. This course will turn out to be very helpful in so many ways.

What is this course, who should take this course and what are the benefits of taking it?
This online course, which is also available for credit from UCI, is designed for medicine and medical assistance students interested in the process of drug development, trials and quality assurance. The main focus of the course is Quality System Regulations and Good Manufacturing Practices as they relate to the field of medicine and pharmaceuticals. During the class you will mainly examine:
- How the U.S. FDA regulates the production and testing of drugs
- Learn the main regulations relating to drug development
- See how these quality systems are applied on the global scale

Table of Contents:
- Introduction
- Essential elements of Quality System Regulations (QSR's) and Good Manufacturing Practices (GMP's)
- How there is a commonality between QSR’s and GMP’s
- How to develop a global approach to Quality Systems in order to satisfy international requirements
- A detailed analysis of these systems and practical 'how to' recommendations and approaches are presented, with particular emphasis on the United States Food and Drug Administration (FDA) QSR's and GMP's

Author Bio
Instructors from the University of California, Irvine will help you in this course.

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