Quality Control - Chemical Analyses
High capacity and short turn around time
The chemical analysis service comprises raw materials, APIs, finished products, packaging material and medical devices. Eurofins Pharma Services have a network of experienced chemists, well-equipped laboratories and well-structured processes allowing us to offer you an exceptional short turnaround time. For example, Eurofins Pharma Services operate more than 15 GC and 40 HPLC chains at our facilities dedicated for chemical analysis. Our high capacity and optimized processes guarantee a fast analyses and reporting of your samples. High quality of results and methods
All documentation is extremely detailed, and fully GMP reviewed at test completion. Because of the stringent checks and balances between the laboratory and the Quality Assurance Group, all results are guaranteed to be accurate and reliable. Our services for raw materials and finished products analysis apply to European, Japanese and American monograph type Pharmacopoeia (EP, JP, USP) and client-supplied methods. This includes the following activities:
- Optimizing and validating of analytic methods
- Measuring of active principle and purity profile of raw materials
- Identification and measuring of degradation products, impurity of synthesis
- Identification and measuring of preservatives in cosmetics
- Identification and measuring of residual solvent
- Studies for the establishment of in vitro bioavailability of the active substance in the most suitable media
- Comparative physical and physico-chemical determinations (e.g. pH, viscosity, melting point, osmolality and osmolarity flash point, loss on drying)
- Limit tests (heavy metals testing, ash, anions)
- Pharmaceutical technical procedures (e.g. disintegration, dissolution, hardness, friability)
- Sampling and analyses of water for pharmaceutical purpose and controlled process environments (e.g. TOC analyzer / testing, conductivity)
- Custom-designed chemical studies following the customer’s requirements