Office 395, Gamarnik-str. 30, 220131, Minsk,
Republic of Belarus
               +375 (29) 551-25-10

Our statisticians are involved in the clinical trial throughout all stages. The correct determination of study design, end-points, sample size and methods of statistical processing is the indispensable prerequisite to obtain reliable results. Clinical study reports prepared by our professionals in conformity with ICH requirements have been approved by the Ministry of Health of the Republic of Belarus.


  • Calculation of sample size
  • Selection of study design
  • Determination of efficacy and safety end-points
  • Statistical analysis plan
  • Case report form
  • Randomization
  • Preparation of interim reports
  • Database creation
  • Data input and double check
  • Statistical processing
  • Preparation of final report of clinical trial

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