Clinical research

In order to conduct a clinical trial, we involve professional expertise in the relevant therapeutic area, use the latest IT solutions and a proactive approach. All this allows you to efficiently search for research centers and recruit patients, increases the efficiency and quality of projects, and also reduces the time of research.
After all, each clinical trial is unique and is based on the therapeutic effect of the investigational drug, the clinical significance of which remains to be investigated and confirmed.
Our database includes more than 150 medical organizations and principal investigators with extensive experience in conducting clinical trials.

Our key competencies:
Drawing up a protocol and other documents of clinical trials;
Monitoring of clinical trials;
Outsourcing of specialists;
Medical experts;
Post-registration safety studies;
Non-interventional studies;
Systematic review

We have established an internal quality management system for clinical trials that complies with all the requirements of good practice and ensures that every project is carried out with the same quality.
We use adaptive design to reduce research time and optimize budget.
We adopt a risk-based approach based on widely used academic and industry initiatives that provide risk-based monitoring tools.
Contact us to find out more.

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