| Sanquin Pharmaceutical Services can provide a testing strategy for each stage of your production process based on mammalian cell technology. Whether you are in need of full characterisation of your seed lot, testing of the bulk harvest and/or the final product, we can offer validated study protocols for all of your testing needs in full compliance with European and FDA-guidelines. For this purpose, we have been awarded a GCLP (Good Control Laboratory Practice) approval as defined in the Guide to Good Manufactoring Practice for Medicinal Products in the European Community. Almost all assays are performed in house under guidance of our highly trained specialists, providing you with the clear advantages of short communication lines and a maximum of commitment. You will find us a reliable partner dedicated to provide you with the test results within the shortest time feasible, while maintaining our prices at a level that can be considered very competitive. | |
After finalisation of the tests, all results are provided to you by means of a QA-audited final report. Please find an overview of all the assays in the menu (on the left side).
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