VALARTIN PHARMA LLC is actively involved in research and development of generic drugs, dietary supplements and medical devices.  

The work is coordinated by the Department of Pharmaceutical Development and Regulatory Affairs, which includes its own Pharmaceutical Development Center and the Registration Department.

The Center is equipped with modern laboratory analytical and technological equipment, has a qualified staff of process engineers and analytical chemists. Pharmaceutical development is carried out in accordance with the international regulatory requirements of GMP and CCI.

The regular functions of the Department are:

• Development of the composition and technology of drug production.
• Development of methods for controlling drugs, as well as intermediates and starting materials.
• Validation of analytical methods for quality control.
• Study of drug stability.
• Formation of a Registration Dossier in the STD format.
• Conducting pilot and industrial testing of technologies at our own and contract production sites.

• Transfer and testing of quality control methods for raw materials, finished products in the quality control laboratory.
• Introduction of medicines / dietary supplements into mass production.
• Registration (re-registration), amendments to the registration dossiers of medicines.
• Legalization of dietary supplements and medical devices.
• Organization of preclinical trials, clinical trials, study of bioequivalence of the investigated medicines, etc.