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It is important to clean pharmaceutical equipment after manufacturing a product so that subsequent products are not contaminated. Removal of previous product residues from production equipment is known as cleaning. If the entire process of cleaning is documented, this is referred to as validation of the cleaning method.
Cleaning validation proves that the cleaning process is effective in removing all product residues that were created, cleaning agents that were used during the cleaning process, and inhibiting the growth of micro-organisms. This process is done as a requirement of regulatory authorities.
Cleaning Validation Basics Manufacturing companies should do this not only to satisfy regulatory authorities but also to ensure that patients are safe.
