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    • Home
    • CliMed Internship June 25
    • 3in1 Diploma
    • 7in1 Impact Diploma
    • Full Course Catalgue
      • Pharmacovigilance
      • Medical Writing
      • Clinical Research
      • Regulatory Affairs
      • CDM Course
      • SAS Programming
      • Industrial Internship
      • RESEARCH PAPER WRITING
      • ICH GCP E6 (R3) Training
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      • Clin Res Cert Course
      • CRA Training
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      • AI IN PHARMACOVIGILANCE
    • Coming Soon
    • Certificate Verification
    • Students Testimonials
    • Workshops & Webinar
      • Webinars
    • Curio Leardership
    • Gallary
    • Contact Us

  • Home
  • CliMed Internship June 25
  • 3in1 Diploma
  • 7in1 Impact Diploma
  • Full Course Catalgue
    • Pharmacovigilance
    • Medical Writing
    • Clinical Research
    • Regulatory Affairs
    • CDM Course
    • SAS Programming
    • Industrial Internship
    • RESEARCH PAPER WRITING
    • ICH GCP E6 (R3) Training
    • Medical Coding
    • Clin Res Cert Course
    • CRA Training
    • Data Analysis using SPSS
    • AI ML Diploma
    • AI IN PHARMACOVIGILANCE
  • Coming Soon
  • Certificate Verification
  • Students Testimonials
  • Workshops & Webinar
    • Webinars
  • Curio Leardership
  • Gallary
  • Contact Us

Drug Regulatory Affairs

Executive Diploma in Drug Regulatory Affairs

Six-Months Specialized Skill Development Program to Excel in the Pharmaceutical Industry


The Curio Diploma in Drug Regulatory Affairs is designed to equip participants with the essential knowledge and skills to navigate the pharmaceutical industry's complex regulatory landscape.


Course Highlights 

-100% Live classes, recordings on demand 

-Expert-led training and end-to-end engagement 

-Faculty members & resource persons from top-notch industry 

-100% Placement Assistance 

-Leadership Dialogues & Interactions 

-Personalized Assignments & Interview Preparations 


Who can Attend

-Pharmacy/Medical & Other Life Science Students & Professionals 

-Professionals working in the pharmaceutical industry, such as regulatory affairs specialists, quality assurance professionals, and clinical research associates.

-Individuals interested in understanding the regulatory landscape of the pharmaceutical industry.


Registration Fees: 3999 INR (50% Institution introductory discount on 7999/-)

Last Date of Registration & Course Commencement: 

Inquire on 9380436185 (WhatsApp/Call)


*Access the brochure below in downloads for more information* 

Register Here

Drug Regulatory Affairs Brochure

Executive Diploma in Drug Regulatory Affairs (pdf)Download

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