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    • June-July 2025 Courses
    • Rationalizing Med Con 25
    • Full Course Catalgue
      • CliMed Internship June 25
      • 3in1 Diploma
      • 7in1 Diploma
      • 8in1 Diploma
      • CDM Course
      • Medical Affairs
      • Pharmacovigilance
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      • Clinical Research
      • Regulatory Affairs
      • 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
    • Certificate Verification
    • Students Testimonials
    • Workshops & Webinar
      • Webinars
    • Curio Leardership
    • Gallary
    • Contact Us

  • Home
  • June-July 2025 Courses
  • Rationalizing Med Con 25
  • Full Course Catalgue
    • CliMed Internship June 25
    • 3in1 Diploma
    • 7in1 Diploma
    • 8in1 Diploma
    • CDM Course
    • Medical Affairs
    • Pharmacovigilance
    • Medical Writing
    • Clinical Research
    • Regulatory Affairs
    • 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
  • Certificate Verification
  • Students Testimonials
  • Workshops & Webinar
    • Webinars
  • Curio Leardership
  • Gallary
  • Contact Us

Drug Regulatory Affairs Diploma

Executive Diploma in Drug Regulatory Affairs

Six-Month 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 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: 4999 INR (75% CSR-based discount on 19999/-)


Course Commencement: July 8, 2025

Last Date for Registration: June 30, 2025

Inquire on 9380436185 (WhatsApp/Call)

Register Here

Drug Regulatory Affairs Brochure

Executive Diploma in Drug Regulatory Affairs (pdf)Download

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