Certified Training Program on: Vaccines, Biologics & Biosimilars β Regulatory Affairs & GMP Expectations
Job Overview
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Date PostedJanuary 10, 2026
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Location
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Expiration dateJanuary 16, 2026
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Click to apply:
Job Description
Dear Professionals,
Fortunate-Veda Biologics Trainings is pleased to announce a Certified Training Program on:
Vaccines, Biologics & Biosimilars β Regulatory Affairs & GMP Expectations
High-Level CMC Strategy Principles and Submission-Package Checklist
(GMP / cGMP Perspective)
π
Start Date: 12th January 2026 onwards
π Time: 8:30 PM β 10:00 PM (IST)
π» Mode: Live Interactive Zoom Sessions
π¬ Key Training Topics β Overview
1οΈβ£ Equipment / Instrument Qualification
Case Study: AHU Systems
β’ Qualification principles and documentation flow
β’ URSβDQβIQβOQβPQ lifecycle approach
β’ HVAC and AHU qualification β key parameters and acceptance criteria
2οΈβ£ Cleaning Validation & Regulatory Strategy
β’ Designing cleaning validation studies
β’ MACO determination and worst-case product selection
β’ Regulatory expectations (USFDA, EMA, WHO)
3οΈβ£ Process Validation & Regulatory Strategy
β’ Process validation lifecycle β Stage 1, 2, and 3
β’ PPQ approach and continued process verification
β’ Global regulatory submission considerations
4οΈβ£ Submission Package Preparation
β’ CMC structure and submission checklist
β’ Regional expectations: US, EU, WHO
β’ Documentation practices and regulatory communication
5οΈβ£ ALCOA & Data Integrity Principles
β’ ALCOA+ framework and practical implementation
β’ Common data integrity observations and CAPA examples
6οΈβ£ Cleanroom Area Classification
β’ EU-GMP vs ISO 14644 requirements
β’ Cleanroom qualification and environmental monitoring strategy
7οΈβ£ Stability Studies at Different Stages
β’ Development, registration, and commercial stability programs
β’ Bracketing, matrixing, and accelerated studies
β’ Stability trending and data evaluation for submissions
8οΈβ£ Understanding GxP Systems
β’ Non-GMP, GLP, GDP, GMP & cGMP β overview and applicability
β’ Interrelationship between quality systems and compliance programs
π Who Should Attend
Pharma, Biopharma, Vaccines, Biosimilars, Quality, Manufacturing, CMC, and Regulatory Affairs professionals.
π Certification:
Participants will receive a Certificate of Completion from Fortunate-Veda Biologics Trainings.
π For enrollment and details:
π Website: www.fortunateveda.com
π§ Email: fortuneveda@gmail.com
π± WhatsApp/Call: +91-8603223334
Warm regards,
Fortunate-Veda Biologics Trainings
Empowering Regulatory & GMP Excellence
