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Source: blog.seerpharma.com Gap analyses are critical for assessing the scope, compliance readiness, and resource support within a quality system. It also enables your company to. Gmp sites should maintain a register or master validation plan by listing the. The purpose of the validation master plan is to document the compliance requirements for the site and to ensure that. The validation master plan is a summary of validation strategy.
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Source: www.whitehatsec.com This project is a remediation validation and compliance project management for the transition of computerized systems from the previous system. Accept the system’s inherent risks. Other areas to remain focus during computer system validation. The purpose of the validation master plan is to document the compliance requirements for the site and to ensure that. It also enables your company to.
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