Promotes a system life cycle approach based on good practice.Establishes a common language and terminology.Facilitates the interpretation of regulatory requirements.Suppliers can use GAMP to test for avoidable defects in the supplied system to ensure quality products are produced.For users: GAMP provides a documented assurance that a system is appropriate for the intended use before it goes “live.”.Computer system validation (CSV) following GAMP guidelines require users and suppliers to work together so that responsibilities regarding the validation process are understood.GAMP describes a set of principles and procedures that help ensure that pharmaceutical Software (Like QMS Software, LMS software, DMS software etc.) has required quality. International Society for Pharmaceutical Engineering (ISPE) sets the guidelines for manufacturers and the current Version is GAMP 5.
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