Uzbekistan Joined Medical Device Regulatory Training
Delegates studied international regulatory frameworks for medical technology and devices in Beijing.
Updated on Sept. 26, 2026 in Nutrition
The Uzbekistan delegation participated in the 5th GHWP Academy Training in Beijing to focus on global public health and medical device standards. The program provided a platform for international cooperation regarding the oversight and harmonization of medical technology.
Why it matters
Understanding global regulatory standards is essential for ensuring that medical equipment meets safety and performance requirements for public health. This session allowed participating nations to align their local policies with international best practices.
The 5th GHWP Academy Training convened international stakeholders to review medical device regulations and clinical evaluation processes. The effectiveness of these collaborative regulatory efforts remains subject to future national policy adoption.
The players
Nozim Berdiyev
He is the First Deputy Director of the Center for Pharmaceutical Products Safety.
Center for Pharmaceutical Products Safety
An Uzbek agency responsible for overseeing the safety, quality, and registration of medical and pharmaceutical products.
The details
The training focused on the regulatory frameworks that govern the lifecycle of medical devices, from initial clinical evaluation to real-world evidence application. Participants examined how these structured protocols can be harmonized to ensure consistent safety standards for new technologies across different healthcare systems.
Timeline
September 2026: The 5th GHWP Academy Training was held in Beijing.
Health Landscape
This training session sits within the broader scope of the Global Harmonization Working Party regulatory alignment initiatives. It reflects a growing international trend toward standardizing medical technology oversight to simplify cross-border market access and improve safety.
These regulatory discussions facilitate faster access to safe, high-quality medical devices by ensuring that products have undergone standardized clinical evaluations. If you have concerns about the safety or efficacy of a new medical device, discussing these standards with your doctor is a productive step.
The takeaway
Harmonized medical device regulations aim to improve patient safety by ensuring that technologies meet consistent, high-quality international benchmarks. Keep an eye on local health authority updates regarding new medical device authorizations in your area.
Further reading
Learn more about international health standards and nutrition policy on our Nutrition page.
Source note: This article includes information reported by Ўзбекистон Миллий ахборот агентлиги.
