From biologics and vaccine manufacturing to technology transfer, process validation, and GMP regulations, this lecture provides a practical introduction to the field of biomanufacturing. Delivered at the University of Montpellier on November 20, 2025, it covers drug substance and drug product manufacturing, GMP facility design, biosafety, cleaning validation, and regulatory requirements. 

From bags, bioreactors to connectors, an overview of the principal single use equipment and consumables in the manufacturing of vaccines and biologics.

From cell bank preparation to drug subtance manufacturing, formulation, filling, inspection and packaging,  a short introduction to how vaccines are manufactured.