Analysis of in-process controls

During the change management process of approved manufacturing processes and the validation or performance qualification of manufacturing processes, for biopharmaceuticals in particular, large quantities of samples often accumulate, which cannot be analysed by the control laboratory of the manufacturing plant within the short time required. In this case, we willingly perform the corresponding analysis of intermediate stages up to the finished drug on behalf of our customers, which often includes the analysis of several hundred samples under GMP in a short time frame. A well-structured, efficient laboratory with the possibility of performing several different parameters in parallel is essential here.

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Release analytics
On-going / follow-up studies


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