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Clinical Research

Specificity of the generic drugs output to the market requires a comprehensive assessment of their effectiveness and safety

The examples of the practical organization of medical research of output products can be found in a special section for doctors - Clinical Research.

We have created a step by step method of medical research, allows analyze the possible replacement of the existing standards of treatment the diseases. 


In the course of this analysis the definition of drugs - competitors occurs: analogues and substitutes. Clinical research of drugs of different therapeutic groups is carried out in accordance with the developed standard that requires consistent execution of six stages: 
  1. Preparation of specialists and clinics bases for conducting clinical programs for studying efficiency and safety of drugs at the federal and regional levels. 
  2. The development of research documentation according to the GCP principles. 
  3. Control of clinical programs. 
  4.  Preparation and execution of clinical reports, articles and reports. 
  5. Training for medical products representatives. 
  6. Thematic conferences, symposia, seminars for professionals at the federal and regional levels.


 

 

   
 

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