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Certified Program In Drug Regulatory Affairs - Gratisol Labs

Gratisol Labs is India’s leading Drug Regulatory Affairs Training Institute based in Hyderabad, Delhi, Bangalore, Pune and Mumbai.

  • Duration 60 hours
  • Students Enrolled 54
  • Last Updated June 18th, 2020
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Certified Program In Drug Regulatory Affairs


The Regulatory Affairs department is an important part of the organizational structure of pharmaceutical companies. Internally it liaises at the inter phase of drug development, manufacturing, marketing and clinical research. Externally it is the key interface between the company and the regulatory authorities.

Regulatory Affairs is involved in the development of new medicinal products from early on, by integrating regulatory principles and by preparing and submitting the relevant regulatory dossiers to health authorities. Regulatory Affairs is actively involved in every stage of development of a new medicine and in the post-marketing activities with authorized medicinal products.

Regulatory Affairs contributes essentially to the overall success of drug development, both at early pre-marketing stages and at all times post-marketing. The pharmaceutical industry deals with an increasing number of interesting drug candidates, all of which necessitate the involvement of the Regulatory Affairs’ department. Regulatory Affairs professionals can play a key role in guiding drug development strategy in an increasingly global environment.

Program Objectives

The major objective of this course is to provide an interdisciplinary knowledge of pharmacy and law as applicable in the field of pharmaceutical regulation at National and International levels. The course prepares the students to pursue career in pharmaceutical industry, drug licensing and control authorities, and export-import agencies dealing with the pharmaceuticals.

The focus of the lectures is mainly on:

  • Introduction to Clinical Research
  • Preparations & Planning for Clinical Trials
  • Introduction to Regulatory Affairs
  • Global Regulatory Environment
  • Pharma Regulations Practices & Procedures
  • Import and Export of Drugs in Global Pharmaceutical Industry
  • Common Technical Document
  • Good Manufacturing Practice
  • Quality Assurance and Regulation
  • Regulatory Aspects in Pharmacovigilance
  • Regulations Governing Clinical Trials & New Drugs
  • Global Drug Policy
  • Essential Documentation in Clinical Research & Regulatory Submissions
  • Clinical Trials Project Planning & Management
  • Study Start Up Process
  • Clinical Monitoring Essentials
  • Compliance, Auditing & Quality Control in Clinical Research Program


A candidate seeking admission to the above programme must have passed bachelor degree in pharmacy or medical sciences. A candidate having bachelor Degree in any discipline with two years of experiences in Pharma industry will also be eligible.


To Maintain High Academic Standard, Gratisol Labs Gives Due Importance To The Quality Of Students Enrolled. To Ensure This, The Selection Of Individual Student Will Undergo The Following Procedure:

Personal Interview

Screening And Selection Of Students


Certificate will be provided for this Course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by Gratisol Labs.

A fast track weekend course will also be conducted for employees & aspirants of Clinical Research Industry.

For more information, please contact Gratisol Labs at info@gratisol.com.


Meet your instructors

Gratisol Labs

Gratisol Labs

Subject Matter Expert - Pharmacovigilance

  • Students: 54
  • Duration: 60 hours
  • Effort: 2–5 hours per week
  • Institution: Gratisol Labs LLC & Texas University
  • Subject: Regulatory Affars
  • Quizzes: Yes
  • Language: English
  • Video Subtitle: English
  • Certificate: Yes
  • Module 2- Pharma Patents, IPR and Regulation
    No items in this section
  • Module 3- Pharma Regulatory Regime in USA, EU and India
    No items in this section
  • Module 4- Clinical Trials & Regulation
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  • Module 5- Good Manufacturing Practices, Quality Assurance and Regulation
    No items in this section
  • Module 6- Regulatory Compliance for Pharma and Biotech Products
  • Module 1- Pharma Regulation Practices and Procedure
    No items in this section

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