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30 september 2023 year

Сompletion of the development of the new Digital Medical Device Quality System eMDD-RIMS

We announce the completion of the development of the new Digital Medical Device Quality System eMDD-RIMS. eMDD-RIMS is a document management system for manufacturers, authorized representatives and distributors of medical devices that significantly simplifies the management of regulatory and quality documentation. The system allows you to create a centralized documentation repository with access for all […]

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10 june 2022 year

Database on pharmacovigilance and safety of medicinal products DSBase has received new functionality

The Computerized system “Database on pharmacovigilance and safety of medicinal products DSBase” has received new functionality – the ability to import and export reports on adverse reactions or lack of efficacy of drugs in electronic form in the ICH E2B (R3) format, a format that is currently a standard in the EU. The International Conference […]

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