Events November 29, 2023 Virus safety challenges: get the job done! Virus safety is key in bioprocessing. In this free 1-day seminar you’ll learn how to… admin-element
ArticlesRegulatory August 25, 2023 A risk based approach to sterile filtration Drug quality cannot be assured only by finished-product testing. Process validation is required to... admin-element
ArticlesBioPharmaRegulatory November 16, 2017 Evaluating Surface Cleanliness Using a Risk-Based Approach Regulated companies that use automated cleaning applications have always struggled with correlating... admin-element
ArticlesRegulatory August 13, 2015 Cleaning of Dedicated Equipment: Why Validation is Needed Cleaning of pharmaceutical equipment is essential to reduce the risk of product contamination and... admin-element
ArticlesDownstreamRegulatoryUpstream November 1, 2014 Viral Clearance Challenges in Bioprocessing Removal and inactivation of adventitious and endogenous viruses have traditionally been achieved... admin-element
ArticlesDownstreamRegulatoryUpstream January 13, 2014 PDA’s Technical Report for Biotech Cleaning Validation Cleaning validation plays an important role in reducing the possibility of product contamination... admin-element