ISPE CEUs: 2.0
Type: Classroom Training Course
This course has been updated to include the new revised EU GMP Annex 11, and an update on 21 CFR Part 11.
This three-day fundamental course introduces participants to regulatory requirements for computerized systems in the pharmaceutical industry and explores tried, tested, and internationally recognized methods of meeting those requirements. GAMP guidance provides a pragmatic and effective framework for achieving computerized systems that are fit for intended use and meet current regulatory requirements.
The course does not aim to cover detailed and highly technical aspects of software and hardware engineering, but rather gives the principles and an overview of the overall computer systems compliance process, including a scaleable and efficient system lifecycle, Quality Risk Management , updated GAMP categories, the role of the supplier, and the selection of appropriate specification and verification activities.
Immediately apply the course learning objective with a complimentary copy of the bound GAMP® 5: A Risk-Based Approach to Compliant GxP Computerized Systems Guide and an electronic download of the GAMP Good Practice Guide: A Risk-Based Approach to Compliant Electronic Records and Signatures.
This training course is of particular interest to existing and future members of the GAMP Community of Practice (COP).