GMP is an acronym for Good Manufacturing Practice regulations put in place by the U.S. Food and Drug Administration (FDA). GMP is typically used in facilities where drugs or medication are manufactured. These regulations address a variety of areas, including cleanliness, personnel qualifications and record-keeping, all in an attempt to ensure safety in the manufacture and care of FDA-regulated products by minimizing the chance of contamination or human error. Here are the 10 principles of GMP..!!
