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GUS-LAB - Version VALIDAT -Quality Assurance Laboratory Software
In over 20 years VALIDAT has established itself as the market-leading software solution for efficient method validation. Today, VALIDAT supports our customers in the pharmaceutical, chemical and biotechnical industries, in petrochemistry, materials testing or in the automotive sector with validation documentation that complies with regulations: reliably, professionally and safely. Of course, VALIDAT also fulfills the requirement for full 21 CFR Part 11 compliance.
VALIDAT can be easily integrated into the infrastructure of your company and into your workflows. Installation in a private cloud is just as possible as installation in a public cloud. Measuring devices and other applications can be connected at any time. An interface to LABS/Q® LIMS is also available.
VALIDAT is primarily and ideally suited to validate analytical methods easily and very efficiently. As the market-leading method validation laboratory software, VALIDAT supports you with its sophisticated and comprehensive functionality in method validation; from the planning of a validation project, to the automatic evaluation and reporting.
Method transfer is necessary if tests are to be transferred to other internal or external analytical laboratories. Otherwise, problems with the comparability of the results occur again and again. VALIDAT supports you in the method transfer by stored templates, so that the method transfer can even be planned automatically at the laboratories concerned.
Interlaboratory comparisons are an extremely important element of quality assurance in the laboratory, especially when equivalent products have to be produced and tested in different countries or plants. To check the expected quality, interlaboratory comparisons can be planned across laboratories with VALIDAT and the samples required for this can be sent to the laboratories involved. The collection of the measurement results including the date and status tracking is done by VALIDAT, as well as the automatic statistical and graphical evaluation of the results and the report generation and distribution.
Release testing of pharmaceutical products to predict the bioavailability of an active ingredient is indispensable in the pharmaceutical industry. The dissolution module of the VALIDAT laboratory software enables the planning of these projects as well as the recording of the measured values of release automats and analytical devices. But also the necessary calculations and evaluations, the statistical evaluation and visualization of the results, furthermore the reporting and documentation of the release experiments are made possible with the Dissolution module.