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