Since January 2013, the Independent INVITRO laboratory has provided a full range of services for the organization and conduction of clinical trials.

Preconditions to creation of the CRO were:

• Broad experience of participation in clinical trials
• Good reputation in the market
• Long-term partnership with the pharmaceutical companies (All this allows increased quality and reduced time and expenses of clinical trials, to simplify oversight by the Sponsor and other authorities)
• Development and preparation of study documents
• Regulatory submission (study approval, import/export license)
• Site monitoring
• Legal support during the study