Résultats de la recherche - 5 results
Microbial quality analysis of falsified medicines seized by controling agencies
good manufacturing practices (GMP). The potential health risks associated with consuming such compromised medications range from toxic impurities to contamination with pathogenic microorganisms. In this ...
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 des vaccins et produits sanguins Kwaliteit van vaccins en b ...
Controlled Human Infection Studies: Proposals for guidance on how to design, develop and produce a challenge strain.
followed by use of qualified methods to test critical steps in the manufacturing process, or the final product itself. These activities are complementary: GMP rules, which intervene only at the time of the ...
Impurity fingerprints for the identification of counterfeit medicines--a feasibility study.
medicines are manufactured in non good manufacturing practices (GMP) conditions by uncontrolled or street laboratories. Their chemical composition and purity of raw materials may, therefore, change in the ...
Next-generation sequencing as a tool for the molecular characterisation and risk assessment of genetically modified plants: Added value or not?
Technol., Volume 45, Issue 2, p.319- 326 (2015) ISBN: 0924-2244 Keywords: Genetically modified organism (GMO) Genetically modified plants (GMP) Next-generation sequencing (NGS) Risk assessment Molecular ...