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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.
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.
Fill out the feedback form and we will provide you with a set of documents, which includes: