News
News and regulatory updates
Changes to the Uzbek framework, and notes from our own work.
- guidancePublished:
Preparing for 26 February 2026: a practical checklist
Classification, representative, dossier, e-imzo — what to have ready before the new regime applies.
Read more - guidancePublished:
The Authorized Representative requirement explained
Foreign manufacturers must appoint a locally established Authorized Representative recorded on the State Register.
Read more - regulatoryPublished:
Which approvals qualify for the recognition pathway
Only five reference regulators are recognised: US FDA, EU CE, UK MHRA, Japan PMDA and Korea MFDS.
Read more - regulatoryPublished:
Resolution No. 738 enters into force on 26 February 2026
The new medical device regulation adopted on 24 November 2025 replaces the previous framework and applies from 26 February 2026.
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