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Introduction to Clinical Benefit-Risk Assessment for the evaluation of (new) medicinal products
Monocyte activation test
Vaccine Stability Testing
Risk Management Plan
3Rs Opportunities for Pertussis Vaccines
Sanitation and Hygiene
Vaccine Manufacturer Viability
Three Rs in vaccine development and testing
Transfer of Technology
Good Practices for Quality Control Laboratories
Good Practices for Pharmaceutical Microbiology Laboratories
Preparation for GMP audit: Inspection Process
Post Approval Changes in Biologics Manufacturing
Production Economics for Vaccines
Vaccine pharmacovigilance
Biosecurity measures
Biorisk assessment and evaluation
Introduction to Biorisk: Biosafety & Biosecurity
Common Technical Document (CTD): Usefulness of the CTD for the Registration of Vaccines Globally
Global traceability standards - Barcodes and serialisation for supply chain efficiency
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