– identification of an adverse event;
– receipt of consumer complaints;
– the appearance of counterfeit and counterfeit products on the market;
– the need for a constructive dialogue between the members of the association and government agencies, including control and supervisory services;
– changes in the Russian legislation of the industry.
– Organization of clinical trials, registered medical devices, for the purpose of preparing scientific publications, collecting case studies, presentations at specialized conferences
Expert support (legal, medical, etc.) in cases of: