Overview
Certificate Course in Drug Regulatory Affairs (DRA)
Delve into the crucial aspects of the pharmaceutical industry with this comprehensive Certificate Course in Drug Regulatory Affairs (DRA), offered by Udemy. This course is meticulously designed for professionals eager to enhance their understanding and mastery over critical regulatory documents like NDA (New Drug Application), ANDA (Abbreviated New Drug Application), CTD (Common Technical Document), and DMF (Drug Master File). Participants will gain an in-depth knowledge of regulations by the USFDA, strategies for effective regulatory submissions, Good Manufacturing Practices (GMP), and the essentials of clinical research. The course also explores the pivotal elements of the Orange Book, making it a must-attend for anyone aiming to excel in pharmaceuticals. Perfect for individuals seeking advanced training in Clinical Research Courses.
Syllabus
Taught by
Tags
Udemy
Udemy
2008 Courses
Udemy
Paid Course
English
3-4 hours
On-Demand
Beginner
