Eurofins BioPharma Product Testing Netherlands, fully GMP certified, provide analytical chemical testing solutions for raw materials, drug substances and drug products. Our services range from routine QC testing, such as characterisation, identification and limit tests of compounds, to highly complex methods using combination LC-MS and NMR technologies.
Routine Testing as per PhEur/USP
The following tests are only a small part of our testing services and performed routinely on a large scale basis. We offer various additional services surrounding these processes. If you have any questions regarding our services, please do not hestitate to contact us to find out whether we can help.
- Complete Compendial Analysis (EP, USP, JP, BP)
- Residual Solvents
- Pharmaceutical Water (EP, USP, JP)
- Elemental Analysis
- Container Closure Testing (EP, USP)
- Trace Metals (USP <232> and <233>)
- AA, GFAA
- Fourier Transform-Infrared Spectroscopy
- Loss On Drying
- UV Spectroscopy
- Water Determination by Karl Fischer (Volumetric & Coulometric)
- X-Ray Diffraction (XRD)
Validation of analytical methods per PhEur/USP
Not only can we assist you with routine QC testing, we also offer analytical development and validation services as per PhEur/USP. A validation project comprises a study plan, study design, performance of analytical work and subsequent data handling. All data is presented in a detailed study report.
- Single-point-of-contact. Eurofins BioPharma Product Testing Netherlands has all expertises within the same organization, allowing clear and reliable communication.
- All services available internally. As Eurofins BioPharma Product Testing Netherlands is the mother holding of several complementary companies, all this expertise is brought together in one multidisciplinal organization.
- Standard and custom solutions. If our standard solutions do not fullfil your requirements, our skilled technicians are able to develop specialized solutions. Please contact us if you want to discuss your needs.