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.