Zoekresultaten - 6 results

What do we request for production and quality control of CHIM strains.Should it be GMP or is adherence to GMP acceptable?

Publication Type: Scientific poster, presentation or proceeding Authors: Wim Van Molle Source: Ethical Approval for CHIM Clinical Trial Protocols, IABS, Brussels, Belgium (2023) Service:  Qualité ...

From b to y ions, a decade of experience with peptide and protein analysis

clinical trials. The Belgian Federal Agency for Medicines and Health Products (FAMHP) and customs are striving, together with their global counterparts, to curtail the trafficking and distributions of these ...

Collaborative data collection by TREAT-NMD Registries to support post-marketing surveillance in Spinal Muscular Atrophy

clinical trial readiness and recruitment. In the current SMA landscape there is a need for more widespread longitudinal data collection to support future research and post marketing surveillance (PMS) ...

The Rabies ONEDAY Study: Results of an alternative single visit intradermal pre-exposure vaccination schedule in an open-label randomized clinical trial on rabies boostability

Northern European Conference on Travel Medicine, Issue. (2016) Keywords: alternative an Clinical clinical trial conference European intradermal Medicine ON Rabies result results study Travel Vaccination ...

Regulatory issues regarding manufacture and control of vaccine adjuvants. The EU situation.

at batch release Belgian Change Clinical clinical trial Clinical trials Combination Components Control developing Development distribution EU European future Group Guidelines health Hepatitis Hepatitis ...

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