Extensive testing is undertaken to determine whether the specification of the material has been met and / or to address expected regulatory concerns. These series of tests can also be applied to determine overall drug compatibility or for routine quality control.
Pharmacological monographs such as the US Pharmacopoeia-National Formulary (USP / NF), European Pharmacopoeia (EP) Japanese Pharmacopoeia (JP) and British Pharmacopoeia (BP) provide standard methods and specifications for generic pharmaceutical raw material finishing products.
EUROLABcan conduct analysis of compendia release test for raw materials and drug products on a daily basis to meet specifications.
EUROLAB, with its highly expert team and internationally accredited laboratories, Complementary Tests It performs all test, analysis, measurement, evaluation and report generation services completely and reliably.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.
