QMS stands for "quality management system." In the pharmaceutical industry, a QMS is a set of processes, procedures, and documentation that are used to ensure that products are consistently produced and controlled to the required quality standards. A QMS helps a company to plan, implement, review, and improve its quality management activities, with the goal of meeting customer requirements and regulatory standards.
In the pharmaceutical industry, QMS is an important aspect of drug development, manufacturing, and distribution. QMS practices are regulated by national and international standards, such as the International Organization for Standardization (ISO) 9001 standard and Good Manufacturing Practice (GMP) guidelines. QMS practices may include activities such as quality control, quality assurance, quality improvement, and quality risk management.
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