Posts Tagged ‘Bioprocess Systems’




Requalification – GMP-requirements for the pharmaceutical industry are valid worldwide

The initial achieved qualification status has to be maintained durably. For this purpose, relevant influencing factors on General Manufacturing Process (GMP) have to be checked periodically. The regulatory requirement of requalification is mandatory worldwide. Prominent superordinate regulations are the GMP guidelines of the US and the EU as well as the guidelines of PIC/S. …more



Bosch at BioProcess International

Join Bosch at BioProcess International in Boston, Massachusetts October 26 – 29, 2015.

We will be featuring our capabilities in process systems for pharmaceutical liquids — which includes bioprocess systems for blood plasma fractionation and bio API manufacturing, preparation and formulation systems for liquids, and generation systems for high purity media. …more


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