Job Description

🚀Exciting News! A New Batch Is Starting Soon!

🧬Embark on a journey of knowledge with our comprehensive course on Vaccines, Biologics & Biosimilars Regulatory Affairs, focusing on CMC (Chemistry, Manufacturing, and Controls) and Filing Strategies.

🧬 We are delighted to offer Free 5-Day Virtual Demo Sessions, giving you a sneak peek into the course content and structure.

This is a fantastic opportunity to explore the intricate world of Vaccines, Biologics & Biosimilars Regulatory Affairs and gain valuable insights into CMC and Filing Strategies. Don’t miss out on this chance to enhance your understanding and expertise in this rapidly evolving field.

Vaccines, Biologics & Biosimilars Regulatory Affairs: CMC & Filing Strategies Course
📅 Dates: 8th –12th December 2025 (Mon–Fri)
⏰ Timings: 8:30 – 10:00 PM IST
🌐 Mode: Online (Live & Interactive via Zoom)

🔍 What You’ll Learn in the Free Sessions
✔️ Regulatory landscape for biologics & biosimilars
✔️ CMC (Chemistry, Manufacturing & Controls) requirements
✔️ Filing strategies for US FDA, EMA, WHO, CDSCO & global agencies
✔️ Common pitfalls in regulatory submissions
✔️ Live Q&A with industry experts

👩‍🎓 Who Can Attend Free Demo Sessions?
This program is ideal for:
🎓 Students & Fresh Graduates in life sciences, pharmacy, biotechnology, and related fields aspiring to enter Regulatory Affairs.
🏭 Industry Professionals working in R&D, QA/QC, Production, or CMC who want to transition into Regulatory Affairs.
📑 Regulatory Affairs Associates/Executives seeking deeper expertise in biologics, biosimilars, and vaccines.
🧪 Academicians & Researchers interested in regulatory compliance for translational research.
🌍 Anyone aiming for a career in global regulatory submissions and CMC documentation authoring, please contact below immediately

📞 Contact Us to Register
📱 Phone/WhatsApp: +91-8603223334/ +91-7680968997
📧 Email: fortuneveda@gmail.com
📧 contact@fortunateveda.com