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PLM good manufacturing practice (GMP)

PLM good manufacturing practice (GMP) refers to the guidelines and regulations set by the regulatory authorities for the manufacturing of products, particularly in the pharmaceutical and medical device industries. These guidelines and regulations are designed to ensure that products are consistently produced and controlled to the quality standards appropriate for their intended use, and that they meet the requirements of the relevant regulatory authorities.

GMPs cover areas such as facility design and maintenance, equipment validation and maintenance, process validation, documentation and record-keeping, and personnel training. The goal of GMP is to ensure that products are consistently manufactured to high quality standards, and that they are safe and effective for their intended use.

PLM GMP is related to the management of product lifecycle, it covers the whole process of product development, production and distribution. This includes the GMP guidelines and regulations in order to ensure that the product is manufactured under a controlled environment, and that the product is safe and effective for its intended use.

PLM GMP can be integrated with the EDMS to ensure that all the documents and information related to the product development, production and distribution process are in compliance with the GMP guidelines and regulations. This can help to ensure that the product is manufactured under a controlled environment and that the product is safe and effective for its intended use.

In summary, PLM Good Manufacturing Practice (GMP) is a set of guidelines and regulations set by regulatory authorities for the manufacturing of products, particularly in the pharmaceutical and medical device industries. These guidelines and regulations are designed to ensure that products are consistently produced and controlled to the quality standards appropriate for their intended use, and that they meet the requirements of the relevant regulatory authorities. It covers the whole process of product development, production and distribution, and it can be integrated with the EDMS to ensure compliance with GMP guidelines and regulations.

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