Tashkent, Uzbekistan (UzDaily.uz) — Uzbekistan and China have discussed the regulation of medical devices, including state registration, regulatory reviews, and assessments of product quality and safety, the Pharmaceutical Products Safety Center under Uzbekistan’s Ministry of Health said.
The meeting was held at the center with specialists led by First Deputy Director Nozim Berdiev, representatives of the China Association for Medical Devices Industry (CAMDI), and Chinese medical device manufacturers.
Participants were briefed on Uzbekistan’s legal requirements governing the circulation of medical devices. Particular attention was given to product registration procedures, regulatory reviews, and assessments of compliance with established quality and safety standards.
The sides also exchanged views on the development and regulation of modern medical device technologies, international experience, and opportunities to expand practical cooperation between relevant organisations in Uzbekistan and China.
Founded in 1991, CAMDI brings together around 4,000 participants involved in the development, production, testing and certification of medical devices, as well as specialised education.
The association contributes to the development of China’s medical device industry, supports innovation, and promotes international ties in the sector.
