Cleaning validation is a necessary and time-consuming part of the pharmaceutical manufacturing process. Cleaning validation is a requirement in pharmaceutical production that adheres to Good Manufacturing Practice (GMP) and Quality Systems Regulations (QSR). Simply put, validation is a documented guarantee that cleaning can be performed reliably and repeatedly to achieve a specified level of purity. Validation is achieved by demonstrating at least three times that the cleaning process removes residues to an acceptable level.
What you should know about pharmaceutical cleaning validation
Mar 23, 2020 | Manufacturing Process