Whitepaper: Cleaning validation
Posted: 22 July 2021 | Reading Scientific Services Limited | No comments yet
This whitepaper discusses cleaning validation and the considerations required for a successful outcome.
The data used to determine the success of a cleaning validation is built upon both the effective evaluation of the manufacturing plant and the robustness of the validated analytical method. This whitepaper discusses the over-arching strategy for performing a successful cleaning validation, with detail on some of the key factors to consider at both the manufacturing, microbiological and analytical stages, highlighting many common pitfalls to avoid.
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Analytical techniques, Biologics, Biopharmaceuticals, Biosimilars, Environmental Monitoring, Gene therapy, Good Manufacturing Practice (GMP), Manufacturing, Medical Devices, Microbiology, Outsourcing, Proteomics, QA/QC, Regulation & Legislation, Research & Development (R&D), Stem Cells, Vaccines