Statistical analysis of clinical trial data

Responsibility for the statistical part of clinical trials rests with biostatistics. Biostatisticians are part of the study design team and are the authors of the most important clinical study documents, including the statistical analysis plan and the statistical report. Our specialists can assist in the development of design, selection of randomization methods, selection of endpoints of the study, determination of the required number of patients / volunteers to obtain a statistically significant conclusion, directly during the analysis of the results obtained, the formation of a conclusion and the preparation of the final report on the results of clinical trials.

"Turnkey" Project

You can provide only the molecule name, and we will develop the entire strategy for bringing the drug to market: from designing, calculating the sample size, selecting a reference drug, its procurement (in the Russian Federation or import), to writing the final report on the conducted research and submitting it to regulatory authorities.

Optimal speed and quality of services

Full compliance with international norms and standards

Logistical availability

Risk reduction and rapid response