The services of Eurofins BioPharma Product Testing Netherlands are not limited to small scale GMP manufacturing. We strive to be your partner in the entire process, so if your project requires additional services or customisation, please contact us to discuss the possibilities.
With a flexible approach, Eurofins BioPharma Product Testing Netherlands is able to work with primary packaging materials, raw materials, and excipients delivered by clients.
If requested, Eurofins BioPharma Product Testing Netherlands can also purchase and release all materials for the manufacturing activities. Raw materials and excipients will be tested and qualified according to the current pharmacopoeia (EP/USP).
All primary packaging components contain constituents such as impurities, contaminants, and degradants that have potential to accumulate in the end product. These constituents are typically referred to as extractables and leachables. Eurofins BioPharma Product Testing can perform extractable and leachable studies. State-of-the-art equipment is available to perform testing to identify and quantify extractables and leachables in your pharmaceutical product.
Eurofins BioPharma Product Testing Netherlands can develop and validate the required GMP compliant test methods to perform in process controls during your manufacturing process, as well as the release testing for your batch release.
Our manufacturing department is complemented by a well-equipped chemical and microbiological QC testing facilities.
Design and performance of your stability studies, or development and validation of stability testing methods. Eurofins BioPharma Product Testing Netherlands is your partner for stability studies.
Eurofins BioPharma Product Testing Netherlands can support your entire stability study from study design to storage, monitoring, analytical testing, and documentation. A complete range of storage conditions in climatic chambers, refrigerators, and freezers is available.