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US Regulatory Strategy for Biologics & Pharmaceutical Drugs

Learners: 361

Instructor: Brandon Too

Duration:

This course provides a comprehensive overview of US Food & Drug Administration (FDA) regulations for biologics and pharmaceutical drugs. It is beneficial for scientists, physicians, entrepreneurs, public health professionals, industry analysts, consultants, and biomedical students interested in the biotechnology and pharmaceutical industry. Learners will gain an understanding of the importance of FDA regulations for public health, and how to navigate through the FDA regulations to market a biologic or pharmaceutical. They will also develop their ability to conduct regulatory intelligence and develop a regulatory strategic plan. This course is a great opportunity to gain knowledge of the drug development process and the key regulatory steps toward FDA approval.▼▲

Course Feature Course Overview Course Provider

Go to class

Course Feature

Cost:

Paid

Provider:

Udemy

Certificate:

Paid Certification

Language:

English

Start Date:

2017-01-01

Course Overview

❗The content presented here is sourced directly from Udemy platform. For comprehensive course details, including enrollment information, simply click on the 'Go to class' link on our website.

Updated in [July 27th, 2023]

This course provides learners with an understanding of the importance of US Food & Drug Administration (FDA) regulations for public health, and how to navigate through the FDA regulations to market a biologic or pharmaceutical. Participants will gain knowledge of the drug development process and the key regulatory steps toward FDA approval, as well as develop their ability to conduct regulatory intelligence and develop a regulatory strategic plan. This course is beneficial for scientists, physicians, entrepreneurs, public health professionals, industry analysts, consultants, and biomedical students interested in the biotechnology and pharmaceutical industry.