We offer high-quality analytical services and quality control of active ingredients, excipients and finished drugs under GMP conditions. The instrumentation includes HPLC-UV, HPLC-DAD, HPLC-MS, HPLC-hrMS, HPLC-MS/MS, UV, IR, CE-SDS, CE-UV, CE-DAD, CE-MS, ultra-high-resolution mass spectrometry as well as moisture analysis by Karl-Fischer (volumetric, coulometric, oven technology). In addition, our service includes rheological characterization for formulation development of semi-solid and solid formulations (oscillating and rotating).
We have a profound knowledge, labs as well as the technical equipment to perform the necessary analytics within the scope of drug development and drug manufacturing for products in the clinical phases as well as commercial products. The product release is performed by our own QP staff of PSM GmbH. We also offer these analytical services as part of contract services for products that are not developed or filled in-house.
Our service portfolio includes the following points:
- HPLC (UV/VIS, DAD)
- Particle size detection
- Zeta Potential
- Water content
- Leak Test
- Elemental impurities
- Identity verification acc. to Ph. Eur
- In-vitro drug release (Apparatus II)