Regulatory Requirements for Pharmaceutical Products – A Course for Basic Learning Learn more

- Are you a student or professional related with the field of medicine?
- Do you want to know the ins and outs of the legal side of pharmacology?
- Are you seeking an online course regarding regulatory requirements for pharmaceutical products?
If this is the case then you have come to the right place. The package here contains a course that has been designed to give you the basic tips and information about strategic planning for health products and clinical trials. This course will turn out to be very useful in so many ways.

What is this course, who should take this course and what are the benefits of taking it?
Structured as a series of lessons on topics like strategic planning for health products and clinical trials, this online course is a good starting point for learning the ins and outs of the legal side of pharmacology. This course not only offers lecture notes and topic coverage, but also provides self-assessments and lesson summaries to make sure you understand the material presented. The course is designed for undergraduate students, though some background on clinical research, medical law, and business can help you get more out of the course.
Medical students and people related with pharmaceutical products can get benefit from this course.

Table of Contents:
- Introduction
- 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)
- FDA inspections
- Labelling
- Advertising of medical products
- Preparing Food and Drug Administration (FDA) submissions

Author Bio
Instructors from the University of California, Irvine will help you better understand the contents of this course. The teaching experience of these instructors is expected to benefit the users in every possible way.

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