Certified Training Program on: Vaccines, Biologics & Biosimilars – Regulatory Affairs & GMP Expectations

April 9, 2026

Job Overview

Job Description

Dear Professionals,
Fortunate-Veda Biologics Trainings is pleased to announce a Certified Training Program on:
Vaccines, Biologics & Biosimilars – Regulatory Affairs & GMP Expectations
High-Level CMC Strategy Principles & Submission Package Checklist
(GMP / cGMP Perspective)
πŸ“… Start Date: 10th April 2026 onwards
πŸ•˜ Time: 8:30 PM – 10:00 PM (IST)
πŸ’» Mode: Live Interactive Zoom Sessions



Key Learning Areas
Stability studies at different stages:
Development, registration, and commercial stability programs
Bracketing, matrixing, and accelerated studies
Stability trending and data evaluation for regulatory submissions
Interrelationship between quality systems and compliance programs
High-level CMC strategy and submission readiness

Who Should Attend
Professionals from:
Pharma & Biopharma
Vaccines & Biosimilars
QualityAssurance & QualityControl
Manufacturing & Process Development
CMC & Regulatory Affairs



Certification
Participants will receive a Certificate of Completion from
Fortunate-Veda Biologics Trainings

Enrollment & Contact Details
🌐 Website: www.fortunateveda.com
πŸ“§ Email: fortuneveda@gmail.com
πŸ“± WhatsApp/Call: +91 79842 75451
πŸ‘€ Contact Person: Shipra Trivedi, Training Coordinator

Certified Training Program on:
Vaccines, Biologics & Biosimilars – Regulatory Affairs & GMP Expectations