Clinical studies
Our team contributes to the expansion of the number of clinical studies conducted in accordance with international standards in the Russian Federation and the CIS:
- Creation of expert councils in the field of clinical trials within the framework of project offices in coordination centers in the CIS member states
- Formation of expert councils in the field of clinical trials within the framework of project offices in the CIS member states
- Expert analysis of the organization of clinical trials in the CIS member states
- Analysis of supranational and national legal regulation in the field of clinical trials
- Development of proposals for the harmonization of national legislation in the CIS member states in the field of clinical trials
- Development of proposals for national legal systems to amend and supplement legislation in the field of clinical trials
- Creation of national infrastructures for conducting clinical trials, their regional integration and interaction with international infrastructure networks for clinical trials and other international organizations in this area
- Creation of platform technology (for collecting and managing information, training specialists, conducting bioethical expertise, etc.) for clinical trials in the CIS member states
- Development of Methodological recommendations on clinical trials for the CIS member states
- Creation of a training course on clinical research (for doctors)
- Creation of a training course on clinical research for researchers (full course)
