CAREER AMBITIOUS

PROFESSIONAL DRUG REGULATORY AFFAIRS PROGRAM

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Professional Drug Regulatory Affairs Program Description

Overview

The Professional Drug Regulatory Affairs Program is designed to provide comprehensive training and knowledge to individuals aiming to excel in the field of drug regulation. This program is tailored for both freshers and experienced professionals, equipping them with the necessary skills to navigate the complex regulatory environment of the pharmaceutical industry.

Eligibility :
Our program is open to candidates from a diverse range of academic backgrounds, including:

  • Pharmacy Degrees: B.Pharm, M.Pharm, and Pharm.D.
  • Science Degrees: B.Sc., M.Sc., and Ph.D. in Biotechnology, Microbiology, Biochemistry, Nursing, and related fields.
  • Engineering Degrees: B.E., B.Tech., and M.Tech. with specializations in Biotechnology or Biomedical Engineering.
  • Medical and Health Sciences: BPT (Bachelor of Physiotherapy), MPT (Master of Physiotherapy), BDS (Bachelor of Dental Surgery), BAMS (Bachelor of Ayurvedic Medicine and Surgery), BHMS (Bachelor of Homeopathic Medicine and Surgery), and MBBS (Bachelor of Medicine, Bachelor of Surgery).

Modules :

PROFESSIONAL DRUG REGULATORY AFFAIRS PROGRAM SYLLABUS

Professional Drug Regulatory Affairs Program Modules

    1. Introduction to Drug Regulatory Affairs
    2. Drug Development Process
    3. Regulatory Submissions and Documentation
    4. Good Regulatory Practices (GRP)
    5. Pharmacovigilance and Risk Management
    6. Global Regulatory Strategies
  • Industry Relevant Soft Skills Training

Detailed Syllabus Available

For a comprehensive overview of our syllabus, please reach out to our expert. Detailed information will be provided through our informative brochure.

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Framework Of Success
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Common Profiles / Company after Professional Drug Regulatory Affairs Program

Career Profiles After Completing the Professional Drug Regulatory Affairs Program

    1. Regulatory Affairs Specialist
    2. Regulatory Affairs Manager
    3. Regulatory Affairs Associate
    4. Regulatory Affairs Consultant
    5. Quality Assurance Specialist
    6. Clinical Research Coordinator
    7. Pharmacovigilance Officer
    8. Compliance Manager
    9. Regulatory Documentation Specialist
    10. Regulatory Submission Coordinator

Several companies in India hire skilled professionals after they complete Clinical Data Management (CDM) training from institutes. These companies include:

Cognizant, Tata Consultancy Services (TCS), Accenture, IQVIA (formerly QuintilesIMS), Biocon, Wipro, Syneos Health, Parexel, ICON Clinical Research, CROMSOURCE, Novartis, Pfizer, Sun Pharma, Dr. Reddy’s Laboratories, Lupin, Cipla, Zydus Cadila, Glenmark Pharmaceuticals, AstraZeneca, Mphasis, HCL Technologies, Infosys, Eli Lilly, Novo Nordisk, GSK (GlaxoSmithKline), Jubilant Life Sciences, Cliantha Research, PPD (Pharmaceutical Product Development), Medpace, Siro Clinpharm, PRA Health Sciences, Lambda Therapeutic Research, GVK Bio, KCR Clinical, Covance (LabCorp Drug Development), KPS Life, Veeda Clinical Research, Hetero Drugs, Aurobindo Pharma, Fortrea, Axxonet System Technologies, ArisGlobal, Indegene, Max Neeman International, Pharm-Olam International, Navitas Life Sciences, Ecron Acunova, Jubilant Biosys, Tech Mahindra, and Clintec International are some of the companies in India

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