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Continued process verification (CPV)

To ensure that a commercial biomanufacturing process is in a state of control, life science companies must create and successfully execute initiatives to meet continued process verification (CPV) and other monitoring guidelines.

Clean TeQ Water wins top accolade at IChemE Awards

Clean TeQ Water wins top accolade at IChemE Awards
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Integrated Tools For Upstream Process Intensification Part I

Changes to bioprocessing methodologies in the biopharmaceutical industry are being driven by the need for increased speed, a lower cost of goods.

03 16 21 -- Advancing Sterile Processing With Closed Systems And Single-Use Technologies

03.16.21 Advancing Sterile Processing With Closed Systems And Single-Use Technologies     Looking to scale up your liquid bioprocessing and decrease transfer times? Learn how high-flow, genderless, large-format connectors make scale and efficiency easy and reliable.   It is critical the single-use sterile connectors you select meet the sterility and reliability needs of your application, as minimizing the threat of contamination using a closed system is essential.   The secure, leak-free connection of sensors to single-use assemblies is paramount in ensuring both the accuracy of the measurements taken and protection of the manufacture of expensive drug products.   When considering your time and the threat of how extractables could impact cells and the effectiveness of the therapy, it is worth taking a look at how aseptic connectors compare to traditional tube welding methods.

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