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Guidelines

GAMP 5 Qualification Practices in Pharmaceutical Software Qualification

GAMP 5 (Good Automated Manufacturing Practice) is a guideline developed by the International Society for Pharmaceutical Engineering (ISPE) for the validation of automated systems in the pharmaceutical industry. It provides a framework for ensuring that software and automated systems are fit for their intended use and comply with regulatory requirements.

Guidelines

GAMP 5: The V-Validation Model

The V-Model is a widely used framework in the validation process for pharmaceutical software and automated systems. It provides a structured approach to ensure that systems are developed, tested, and validated in a way that meets regulatory requirements and ensures product quality, patient safety, and data integrity. The V-Model is particularly aligned with the GAMP 5 guidelines and emphasizes a lifecycle approach to validation.