Nov 2026: POST GRADUATE DIPLOMA IN REGULATORY AFFAIRS

Job Description

NEW ONLINE DIPLOMA COURSE – ENROLL NOW!
Dear Sir/Madam,
Greetings from Fortunate-Veda RA Trainings!
We are pleased to announce the launch of our Online Diploma in Drug Regulatory Affairs – Biologics, Biosimilars & Vaccines, designed for professionals and aspiring candidates seeking practical knowledge in global Regulatory Affairs and CMC submissions.
🎓 Diploma in Drug Regulatory Affairs
Biologics | Biosimilars | Vaccines
📘 Focus Areas:
CTD / ACTD / eCTD Dossier Preparation & Global Regulatory Submission Strategies
📅 Course Start Date: 09 November 2026
🕘 Session Timings: 08:30 PM – 10:00 PM IST
📚 Duration: 30 Hours
💻 Mode: Live Interactive Online Zoom Sessions
📌 Course Highlights
✅ Comprehensive understanding of CTD Modules 1–5 and region-specific regulatory requirements.
✅ Practical training in dossier preparation and global submission strategies for USFDA, EMA, WHO, CDSCO, and other ROW markets.
✅ Regulatory Affairs and CMC documentation practices aligned with global regulatory expectations.
✅ Practical guidance on eCTD submission strategies, lifecycle management, and real-world regulatory case studies.
✅ Suitable for professionals and fresh graduates from Regulatory Affairs, CMC, QA, QC, Manufacturing, R&D, Biologics, Biosimilars, and Vaccines backgrounds.
📞 Registration & Contact
📱 Mobile: +91 86032 23334
🌐 Website: fortunateveda.com
📧 Email: fortuneveda@gmail.com | contact@fortunateveda.com
🎁 SPECIAL OFFER
Interested candidates are welcome to attend one FREE live demo session before enrollment to understand the training approach and course content.
⚠️ Seats are limited. Register early to reserve your place.
We look forward to welcoming you to the program and supporting your career development in Global Drug Regulatory Affairs.
Thanks & Regards,
Fortunate-Veda Team