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Felicity Thomas is Associate Editorial Director of Pharmaceutical Technology, Pharmaceutical Technology Europe, BioPharm International.
November 15, 2021
Patrick Nieuwenhuizen, Senior Manager/Consultant, PharmaLex, discusses changes to regulatory requirements, quality risk management, audits, and operational considerations of aseptic processing.
Global supply chain experts examine implications of the DSCSA as well as topical considerations around the EU's FMD in this serialization video series ft. manufacturing, packaging, software, and regulatory experts.
November 12, 2021
November 03, 2021
Investing in formulation strategies earlier on in development will maximize the chance of success.
Alternative drug delivery approaches are promising, but due to their complexity, they need to be sufficiently justified.
November 02, 2021
Manufacturing capacity expansion is high on the agenda for many bio/pharma companies and service providers in Europe.