What is the purpose of Good Manufacturing Practices (GMP) in the regulation of pharmaceuticals?

Good Manufacturing Practices (GMP) are a set of regulations intended to ensure that pharmaceuticals and related products meet specific standards of quality. GMP is a part of the Washington State Department of Health’s requirements for the manufacture and distribution of pharmaceuticals intended for medical purposes. The purpose of GMP is to ensure that pharmaceuticals are safe and effective for their intended use. GMPs are designed to guarantee the safety, quality, and purity of manufactured products. GMPs specify the proper materials and procedures that must be used throughout the production process. This includes ensuring that adequate raw materials are obtained for the production of pharmaceuticals, as well as to ensure that production processes are consistent and well-controlled. All of these requirements are intended to make sure that pharmaceuticals are manufactured to the same high quality standards. GMPs also ensure that pharmaceuticals are labeled properly, stored properly, and have adequate quality control measures in place. All of these are essential to making sure that the medicine is safe and effective when prescribed to patients. GMPs therefore help to ensure that the pharmaceuticals that are available in Washington meet the highest standards of quality.

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What is the purpose of Good Manufacturing Practices (GMP) in the regulation of pharmaceuticals?

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