100% Discount || Pharma Drug Regulatory Affairs course – DRA 2022

Are you looking for Regulatory affairs Jobs in 2022 and want to make a career in Pharmaceutical Regulatory affairs?

Answer:

If you are looking for Pharma Regulatory affairs course to start career as Regulatory Professional without paying huge amount or money then you are on right platform.

This updated course is for starting career and growing in existing profession as in Regulatory affairs with certificate of completion.

Complete the course as per your free time as life time access is available.

If you are paying more than 5k INR or $15 for private institute/academy then you are in loss.

Please compare the course description and amount you are paying for such course.

Course Details:

The Pharmaceutical industry discovers, develops, produces, and markets drugs or pharmaceutical drugs for use as medications to be administered to patients, with the aim to cure them, vaccinate them, or alleviate the symptoms. Pharmaceutical companies may deal in generic or brand medications and medical devices

Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. …

Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus market the drug.

So, this online course helps Pharmacy Students and Professionals to build their knowledge and skills towards career in Regulatory Affairs.

Regulatory course prepares students to be skilled in the field of global regulatory affairs, and enables existing regulatory affairs professionals to refine and update their knowledge of global regulatory affairs statutes and practices.

Prepare to play a pivotal role in managing the regulatory activities necessary to bring drugs and medical products to market.

Contents of this course :-

A. Basics of Regulatory affairs

1. Basic Regulatory Introduction

2. Career and opportunities in RA

3. Objectives in RA Profession

4. Websites and Usage

5. Intoduction to ICH Guidelines

6. Basic general information about DMF (Drug Master File)

7. DMF preparation and submission

B. CTD & eCTD

8. Module 1

9. Module 2

10. Module 3

11. Module 4

12. Module 5

13. eCTD software demo and eValidation

C. Types of Application

14. IND (Investigational New Drug Application)

15. NDA (New Drug Application)

16. ANDA (Abbreviated New Drug Application)

D. Registration and Submission

17. Introduction to ESG Gateway

18. Overview of Registration Process

19. FDA ESG web interface and electronic submission