Do your employees also spend too much time preparing and reviewing reports?
Scientific staff spend an average of 30 percent of their work time meeting the necessary regulatory reporting requirements. We’ll show you how automated reporting can free up more time for your research.
Are you still working with Excel and looking for a way out of the data chaos?
You still collect your data manually and scattered information makes it difficult for you to evaluate, plan and make decisions? With our flexible laboratory information systems, we have the right solutions for every laboratory workflow and accompany your laboratory on its way to digitization.
Your laboratory operates in a regulated environment and is bound by high regulatory requirements – such as GMP/GLP regulations? Our solutions are ISO 17025, GMP and 21 CFR 11 compliant, giving you peace of mind in meeting regulatory requirements.
Flexible laboratory information management solutions for your laboratory
Based on comprehensive standard functionality, our LIMS solutions support your laboratory processes in an intuitive and practice-oriented way. Thanks to an open architecture, they can be seamlessly integrated into the existing infrastructure and easily connected to other IT systems. ISO 9001:2015 standard certified and compliance compliant (including GAMP guidelines, ISO 17025, GxP standards).
studygen - the reporting tool for automated study reports in the pharmaceutical industry
From data capture to the final approval document, studygen creates complex study reports and approval documents in minutes, automated and in compliance with all international regulations while ensuring data integrity.
5 good reasons to get in touch
Efficiency increase: quality, turnover, costs
Compliance and regulatory security
Ahead of the competition – faster to market thanks to automated processes