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CTIS and RFIs without stress – how to effectively manage communication with regulators? CTIS and RFIs without stress – how to effectively manage communication with regulators?
The clinical trial assessment process in CTIS (Clinical Trials Information System) does not end with the submission of an application. One of the key stages ...
Where and how to register clinical trials, medical device studies, and observational studies? Where and how to register clinical trials, medical device studies, and observational studies?
Registration of studies in public information systems has become a standard in conducting research projects and an important element of scientific transparen...
The Foundation of an Effective Clinical Trial: How to Develop a Strong Study Concept The Foundation of an Effective Clinical Trial: How to Develop a Strong Study Concept
A well-prepared clinical trial concept is a key stage that determines the success of the entire project—scientifically, regulatorily, and operationally. It i...

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The year 2025 was a period of intensive development and consistent strengthening of Biostat Research and Development Center’s position at the intersection of...
New Knowledge Base on Clinical Trials New Knowledge Base on Clinical Trials
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Voice Assistant for Doctors – A New AI Feature in the Medfile Program Voice Assistant for Doctors – A New AI Feature in the Medfile Program
Biostat's developers are launching a Voice Assistant for doctors in the Medfile software designed for medical facilities. This AI-based tool operates in ...
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