The term GMP in the pharmaceutical industry, is a collection of practices, controls and procedures to be documented to ensure that medicines are consistently produced and controlled to the quality standards required. It is the backbone of drug manufacture as it reduces the risk of contamination, mix-ups, deviations and error which could impact product safety and effectiveness.
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This section features articles of practical interest to those involved in the pharmaceutical industry with an interest in GMP. There will be information about GMP principles, SOPs, documentation, equipment, validation, troubleshooting, investigations/calculations, maintenance and compliance topics. The articles aim to assist in the daily work in pharmaceutical manufacturing and to give the reader an understanding of the application of GMP in various functions and regulatory environments.