In response to the rigors of the pharmaceutical market, there is an increasing need for hygienic construction in process equipment. When processing products under sterile or clean room conditions – for example injectables and vaccines – there are different challenges, especially regarding product sterilisation. Mixing would typically occur before sterilisation, but in some instances this is impossible, which places further restrictions on the mixing process.

Silverson has pioneered the concept of “Ultra Hygienic” mixing equipment and has developed a range of Ultra Hygienic mixers designed for CIP and SIP, suitable for pharmaceutical and biotechnology applications, including processing of sterile ingredients. Silverson mixers comply with FDA, cGMP and 3A standards. For more information about this specialised application, please read the report below.

Application reports for the Sterile Processing industry

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Mixing of Sterile Ingredients

To respond to legislative and customer requirements, the pharmaceutical industry is having to ...