Food and Drug Administration expectations for good manufacturing practice (GMP) compliance of manufacturing and related systems.

GAMP itself was founded in 1991 in the United Kingdom to deal with the evolving U.S. GAMP Good Practice Guide: Validation of Process Control Systems.GAMP Good Practice Guide: Validation of Laboratory Computerized Systems.GAMP Good Practice Guide: Testing of GxP Systems.

GAMP Good Practice Guide: IT Infrastructure Control and Compliance.GAMP Good Practice Guide: Global Information Systems Control and Compliance.GAMP Good Practice Guide: Electronic Data Archiving.GAMP Good Practice Guide: Calibration Management.GAMP Good Practice Guide: A Risk-Based Approach to Compliant GxP Computerized Systems.Other publications in the GAMP series include: The second edition (GAMP5) was released in July 2022. The most well-known is The Good Automated Manufacturing Practice (GAMP) Guide for Validation of Automated Systems in Pharmaceutical Manufacture. ISPE has published a series of good practice guides for the industry on several topics involved in drug manufacturing. Several local GAMP COPs, such as GAMP Americas, GAMP Nordic, GAMP DACH (Germany, Austria, Switzerland), GAMP Francophone, GAMP Italiano, GAMP Benelux (Belgium, Netherlands, Luxembourg) and GAMP Japan bring the GAMP community closer to its members in collaboration with ISPE's local affiliates in these regions. ISPE organises GAMP-related training courses and educational seminars. The GAMP COP organizes discussion forums for its members. The goal of the community is to promote the understanding of the regulation and use of automated systems within the pharmaceutical industry. Standard operating procedures (SOPs) are essential for processes that can affect the quality of the finished product.Ī group of pharmaceutical professionals have banded together to create the GAMP Forum, which is now a technical sub-committee, known as the GAMP COP (community of practice) of the International Society for Pharmaceutical Engineering (ISPE). As a result, GAMP covers all aspects of production from the raw materials, facility and equipment to the training and hygiene of staff.

One of the core principles of GAMP is that quality cannot be tested into a batch of product but must be built into each stage of the manufacturing process. More specifically, the ISPE's guide The Good Automated Manufacturing Practice (GAMP) Guide for Validation of Automated Systems in Pharmaceutical Manufacture describes a set of principles and procedures that help ensure that pharmaceutical products have the required quality. Good automated manufacturing practice ( GAMP) is both a technical subcommittee of the International Society for Pharmaceutical Engineering (ISPE) and a set of guidelines for manufacturers and users of automated systems in the pharmaceutical industry.

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