Job Description

New Online Course Launch – Enroll Now! 🚀
🎓 Post Graduate Diploma in Drug Regulatory Affairs – Biologics, Biosimilars & Vaccines
📘 CTD / ACTD / eCTD Dossier Preparation & Global Submission Strategies
🧬 Biologics | Biosimilars | Vaccines
📅 Course Start Date: 25 May 2026
🕘 Session Timing: 8:30 PM – 10:00 PM IST
📚 Total Duration: 90 Hours
💻 Mode of Training: Live Online Sessions via Zoom
📌 Course Highlights
✅ Complete understanding of CTD structure (Modules 1–5) with global regulatory perspectives
✅ Dossier preparation strategies for USFDA, EMA, WHO, CDSCO & ROW markets
✅ Comprehensive CMC documentation and regulatory compliance practices
✅ Hands-on training in eCTD submission, lifecycle management & case studies
✅ Coverage of biologics, biosimilars, vaccines, and global filing expectations
✅ Suitable for Regulatory Affairs, CMC, QA/QC, Manufacturing & Pharma Professionals
🎯 Who Can Attend?
Regulatory Affairs Professionals
QA/QC & Analytical Professionals
CMC Documentation Teams
Biotechnology & Pharmacy Graduates
Professionals working in Biologics, Biosimilars & Vaccines
📞 Registration & Enquiries
📱 +91-8603223334
🌐 Fortunate-Veda Official Website
✉️ fortuneveda@gmail.com
✉️ contact@fortunateveda.com
🔖 Limited seats available. Enroll now to upgrade your global regulatory affairs expertise.