With the aim of improving the system of conducting clinical trials in Ukraine in accordance with international requirements and further harmonizing regulatory legal acts in the field of medicinal product registration with European legislation, by order of the State Expert Center of the MoH of 04.09.2019 No. 150 “On the establishment of a working group for preparing amendments to regulatory legal acts in the field of medicinal product registration and conduct of clinical trials” the relevant working groups have been established, which, as early as 16.09.2019, plan to hold their first working meetings.
Based on the results of the work of these groups, it is planned to develop corresponding draft amendments to regulatory legal acts in the field of registration of medicinal products and conduct of clinical trials, which will be published on the official website for public discussion.
