NEW BATCH ANNOUNCEMENT | POST GRADUATE DIPLOMA IN REGULATORY AFFAIRS

Job Description

NEW BATCH ANNOUNCEMENT | POST GRADUATE DIPLOMA IN REGULATORY AFFAIRS
🎓 Biologics | Vaccines | Biosimilars | ADCs | CMC | Global Regulatory Filing Strategies
We are pleased to announce the commencement of our new batch of the Post Graduate Diploma in Regulatory Affairs (PG-DRA) on 15 September 2026.
This specialized, industry-oriented program is designed for professionals and aspiring Regulatory Affairs specialists who want to build strong expertise in Biologics, Vaccines, Biosimilars, and Antibody–Drug Conjugates (ADCs), with a strong focus on Chemistry, Manufacturing & Controls (CMC) and global regulatory filing strategies.
The program combines regulatory concepts with practical dossier preparation, real-world regulatory scenarios, case studies, and global submission strategies to develop industry-relevant regulatory competencies.
📘 COURSE HIGHLIGHTS
Course: Vaccines, Biologics & Biosimilars Regulatory Affairs – CMC & Global Filing Strategies
📅 Start Date: 15 September 2026
⏰ Time: 8:30 PM – 10:00 PM IST
🌐 Mode: Live Interactive Online Sessions – Zoom
🔎 KEY LEARNING AREAS
• Global regulatory landscape for Biologics, Biosimilars & Vaccines
• CMC documentation and regulatory expectations
• CTD/eCTD dossier structure and preparation
• Global regulatory pathways and filing strategies
• Biosimilar development and regulatory requirements
• Vaccine regulatory considerations
• ADC regulatory and CMC considerations
• Regulatory deficiencies and common submission pitfalls
• Practical approaches to global regulatory submissions
• Regulatory lifecycle management and post-approval changes
• Real-world regulatory case studies and submission scenarios
👩‍🎓 WHO SHOULD ATTEND?
• Pharmacy, Biotechnology & Life Sciences students and graduates
• Regulatory Affairs professionals
• Professionals from R&D, CMC, QA/QC, Manufacturing & Production
• Scientists and researchers working with biologics and biosimilars
• Academicians and industry professionals
• Professionals seeking specialization in Global Regulatory Affairs
🎯 PROGRAM BENEFITS
✅ Industry-oriented regulatory curriculum
✅ Practical understanding of CMC documentation
✅ Exposure to global regulatory filing strategies
✅ Real-world case studies and regulatory scenarios
✅ Interactive live sessions with regulatory experts
✅ Practical insights into dossier preparation and lifecycle management
✅ Career-oriented certification upon successful completion
✅ Enhanced knowledge for opportunities in Global Regulatory Affairs

📞 REGISTRATION & ENQUIRIES
📱 WhatsApp / Phone: +91 86032 23334 | +91 76809 68997
📧 fortuneveda@gmail.com | contact@fortunateveda.com
🌐 www.fortunateveda.com

🔔 Admissions are open for the September 2026 batch.