1.  Drug development, including search of new pharmacologically active substances, study of their properties, development of production technology of pharmaceutical substances, development of drug dosage forms and their production technology;
  2. Preclinical trials of safety and efficacy of drugs in accordance with the rules of Good Laboratory Practice (GLP);
  3. Clinical trials of drugs in accordance with the rules of Good Clinical Practice (GCP);
  4. Compiling a dossier for state registration of a drug;
  5. Technology transfer to a production facility.
  6. Each contract is prepared in accordance with the Customer’s requirements and may include both all required preclinical trials and all phases of clinical trials.

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