Global EEU Market: Preparation is Ongoing
The work on documents required for establishment of a common drug market in the territory of Eurasia Economic Union (EEU) is continuing.
Experts from ministries of healthcare of EEU member-states, representatives of pharmaceutical companies and associations took part in the meeting of the ECE task force on joint approaches to regulation of drug circulation. They considered the proposed versions of the Guidelines on Preparation of Dossier for the Study Drugs for Clinical Trials and Requirements to the Quality of Oral Modified Release Pharmaceutical Forms. These drafts were developed by the task force members from Kazakhstan to harmonize requirements of the Union based on globally established pharmaceutical practices. Besides, projects of Guidelines on drug manufacture validation and Requirements to water used for manufacture of drugs developed by the republic of Belarus were discussed.
The work on the project of requirements for studies of stability of drugs and pharmaceutical substances continues, as these will have to accurately regulate the stage of drug quality study in smallest detail.
Besides, a meeting of college of Eurasian Commission on Economics was held, under leadership of Tigran Sarkisyan, its chair. Some of solutions in the sphere of technical regulation required for effective work in the global market of medical devices in the union member-states, which is to be launched before the end of this year.