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 sterilization. Mixing would typically occur before sterilization, but in some instances this is impossible, which places further restrictions on the mixing process.
Silverson has pioneered the concept of “Ultra Sanitary” mixing equipment and has developed a range of Ultra Sanitary 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 specialized application, please read the report below.
Mixing of Sterile Ingredients
To respond to legislative and customer requirements, the pharmaceutical industry is having to demand ever increasing standards of hygienic…