The test is performed in accordance with the pharmaceutical GMP (Good Manufacturing Practice) standard.
Parameter name:
Residual solvents
Analytical technique:
Gas Chromatography (with FID detection)
Description:
The test involves the quantitative analysis of volatile solvents in the raw material or finished product using an internal carrier gas, most often nitrogen or helium, and a detector supply gas (hydrogen and air).
If you are interested in cooperation, please email contact@mtlab.pl or call +48 577 677 444.
