The test is performed in accordance with the pharmaceutical GMP (Good Manufacturing Practice) standard.
Parameter name:
Content Uniformity
Analytical technique:
HPLC, UHPLC (UPLC), GC, UV-Vis, Titration, gravimetric, others upon consultation
Description:
The test consists of a quantitative analysis of the component in the tested mass or finished form by direct determination (e.g. titrimetric methods) or by using an indirect method (using a standard, e.g. chromatographic techniques). For tablets meeting specific pharmacopoeia conditions, it is permissible to test uniformity by measuring mass and Content (AV value).
If you are interested in cooperation, please email contact@mtlab.pl or call +48 577 677 444.
