Basic info
Industry
pharmaceutical manufacturing
Sectors
Impurity Identification
Release Testing
Characterization
& Cytotoxic Compounds
Elemetal Impurities (ICP-MS
Compendia Testing (USP/EP/BP/JP)
& ICH Q3D
ICH Stability & Storage
(NMR
Dissolution Testing
Reference Standard Qualification
Controlled Substances (Schedule l-V)
XRPD
OES) USP <232>
Method Development & Validation
Particle Size Analysis
& FTIR)
<233>
Highly Potent
Date founded
2016