- 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;
- Preclinical trials of safety and efficacy of drugs in accordance with the rules of Good Laboratory Practice (GLP);
- Clinical trials of drugs in accordance with the rules of Good Clinical Practice (GCP);
- Compiling a dossier for state registration of a drug;
- Technology transfer to a production facility.
Each contract is prepared in accordance with the Customer’s requirements and may include all required phases of preclinical and clinical trials.
