Clinical studies

Bioavailability, pharmacokinetics and analysis of physiological parameters in vivo

The aim of clinical trials is to test the efficacy and safety of drugs, certain forms of treatment, medical interventions or medical devices. The first use of a promising medical treatment in humans should therefore be a clinical trial with the aim of testing the efficacy and tolerability of new therapies. However, such a trial can only take place once sufficient data is available for safe implementation and a positive vote has been received from the relevant ethics committee. In order to minimize external interference, such studies are conducted in a controlled environment. Due to successfully conducted studies in various areas (high blood pressure, dental health, blood sugar levels, bioavailability), we have extensive expertise in all project phases. Thanks to good networking, we can mediate between clinical institutions, doctors, test subjects, companies and scientific partners and thus ensure successful implementation.