Kickstart your career in the fast-growing pharmaceutical regulatory sector with our 6-month industry-focused diploma program. Designed by experts, this course equips you with the practical skills needed to handle regulatory strategies for drugs, medical devices, and biologics in Indian and global markets.
Program Highlights
- Industry-oriented curriculum aligned with current regulatory requirements
- Live online classes conducted by experienced industry professionals
- Hands-on training in dossier preparation and pharmacovigilance tools
- Coverage of ICH E6 (R3) guidelines and eCTD v4 principles
- Insights into Digital Health and AI/ML regulatory frameworks
- Capstone project, mini-internship exposure, and interview preparation
Why Should You Enroll?
- Industry-Relevant Skills – Learn practical regulatory strategies used in the pharmaceutical, biotech, and medical device industries.
- Hands-On Experience – Work on real dossier preparation and regulatory tools to gain practical exposure.
- Learn from Experts – Live online sessions conducted by experienced industry professionals.
- Updated Global Guidelines – Get trained in ICH E6 (R3) and eCTD v4 principles, essential for global regulatory submissions.
- Career-Focused Training – Includes capstone project, case studies, and interview preparation to help you enter the industry confidently.
- Exposure to Emerging Areas – Understand digital health and AI/ML regulatory frameworks shaping the future of healthcare.
Program Structure
- Duration: 6 Months
- Total Training: 240 Contact Hours
- 45% Lectures | 35% Hands-on Labs | 15% Case Studies | 5% Industry Talks
Next Batch
Classes Start: 15 April 2026
Mode: Live Online SessionsGlobal Diploma_Poster
Fees
Enroll by paying 10% of the total fee
Program Fee: ₹20,000 (EMI option available)
Gain practical regulatory knowledge, build industry-ready skills, and step confidently into the global regulatory affairs field. ENROLL NOW!!
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