Our Validation Master Plan application is FDA 21 CFR Part 11 compliant
GxpManager’s VMP (Validation Master Plan) application allows you to manage all the validation/revalidation data and activities of your site (equipments, buildings, processes and systems).
- You map your site in a dynamic way. You define, plan and follow your validation activities.
- You strengthen the operations traceability and the tracking of your qualified statuses, and you guarantee that you are up to date with your validation plans.
- You monitor your activity in real time thanks to the dashboards and indicators.
- Your Validation Master Plan is published in one click.
FDA 21 CFR part 11
Audit Trail
Tracking changes to ensure integrity and coherence of data that is subject to standard rules and regulations.
Automatic Publishing of Reports
Create, automatically publish and record personalized reports.
Statistics
You can create and view numerous types of graphic reprezentations for analysing your data in real time, including calculation formulas
Traceability Matrices
You can define matrix for traceability (simple or star shaped) with a data overall vision (specifications, tests, regulations… coverage).
360° View
Allow to obtain an immediate visualization of the chain of links associated with a record (links in all directions).
Validation Master Plan
During this webinar you will discover how GxpManager can help you to simplify, digitalize, and secure your VMP.
Learn moreUnused equipment valuation
Alongside an activity interruption program for which GxpManager provided a project management application
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