Pharmaceutical Testing services
QACS is a GMP & GLP certified lab and provides Pharmaceutical testing analysis services for quality control, design, research and development of proprietary medicines. Testing methodologies stay in accordance with EMA & FDA. QACS is equipped with Microbiological, Chemical and Molecular laboratory premises to provide a variety of Pharmaceutical testing services, solutions and protocols. We also develop and implement validation protocols to document method suitability. Pharma validation services include:
Equipment & Routine Testing
- HPLC with UV or diode array detectors
- UPLC with diode array detectors
- UPLC-MS/MS with diode array detector
- GC with Split/Splitless injectors, FID detectors and liquid injection
- GC with Headspace injector and FID detector
- GC-MS with Split/Splitless injectors, liquid or Headspace injection
- GC-MS/MS with Split/Splitless injectors, liquid, Headspace or SPME injection
- FTIR with ATR
- Atomic Absorption Spectrometer (Flame and Furnace)
- ICP-MS
- UV Spectrophotometer
- Karl Fischer Volumetric and Coulometric Titrators
- Potentiometric titrator
- Nitrosamines according to E.P. 2.5.42
- Method transfer
- Method development
- Method validation
- Genotoxic impurities (e.g. azido impurities in losartan)
- ICH Stability storage and testing
- Residual Solvents in raw materials and API
- Ethylene oxide and dioxan according to E.P. 2.4.25
- Water content by Karl Fischer volumetric or Coulometric Titrations (E.P. 2.5.12 and E.P. 2.5.32)
- Dissolution (E.P. 2.9.3)
- Disintegration (E.P. 2.9.1)
- Assay by HPLC, GC or potentiometric titration
- Related substances by HPLC or GC
- Viscosity (E.P. 2.2.9 or 2.2.10)
Bespoke pharmaceutical testing services are also applied. If you are based in the EU, we offer 24-hour courier service.
To learn more about how Pharmaceutical testing can assist drug production & development, fill in our contact form and find out how QACS supports drug production.