Guidance for Cleaning, Disinfection and Sterilization of Reusable Medical Devices
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29:44
Reprocessing Rethought: An Open Forum Discussion On Novel Decontamination Methods for Reusables
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53:05
USP 665 and 1665 Extractables for Components in Pharmaceutical and Biopharmaceutical Manufacturing
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28:51
Impact of radiation sterilization on single-use products
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27:24
Assuring Viral Safety of the Biopharmaceutical Process
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36:56
Updates to ISO-18562:2024 - A CRO Point of View
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25:38
Qualification of Single Use Materials for Biopharmaceutical Manufacturing
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33:14
Considerations for Validation of Filters used in (Bio)Pharmaceutical Manufacturing
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35:50