Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course

Empowering Professionals in the Pharmaceutical Industry: A Comprehensive Online Course in Drug Regulatory Affairs
4.10 (5 reviews)
Udemy
platform
English
language
Science
category
instructor
Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course
23
students
1.5 hours
content
Sep 2024
last update
$109.99
regular price

What you will learn

Overview of Drug Regulatory Affairs in Pharma Industry

Different terms used in Pharma Industry by Regulatory Professional, which will help in the Regulatory Affair career

Historical Perspective of Drug Regulatory Affairs and different challenges

Journey of Drug from Discovery to Marketing

Drug Composition and Formulation

Different documentations : IND, NDA, ANDA, BLA

CTD and eCTD (Common Technical Document)

Dossiers

ESG and ESG web interface

Drug Registration

API ( Active Pharmaceutical Ingredients) and Excipients , DMF (Drug Master File)

Regulatory Compliance and Agencies

Different Clinical Trials In pharma industries

Approvals of Drug for Marketing

Pandemic Situations Approval of Drugs

Course Gallery

Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course – Screenshot 1
Screenshot 1Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course
Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course – Screenshot 2
Screenshot 2Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course
Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course – Screenshot 3
Screenshot 3Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course
Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course – Screenshot 4
Screenshot 4Pharmaceutical Drug Regulatory Affairs (DRA) 2024-25 Course

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5331680
udemy ID
17/05/2023
course created date
27/05/2023
course indexed date
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