The Resolution 738 reset
Resolution 738 (effective 26 Feb 2026) rewrites state registration — with 4 safety levels and clinical-trial-backed decisions under Decree PF-137.
Free field guide · PDF
Resolution 738, the 155-working-day clock, and the 5-year certificate — with dossier language and practical notes.
Sourced from Uzbek regulatory guidance and verified 2026 publications.
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What's inside
Every figure in this guide traces to a named source — Uzbek regulatory guidance and verified 2026 publications.
Resolution 738 (effective 26 Feb 2026) rewrites state registration — with 4 safety levels and clinical-trial-backed decisions under Decree PF-137.
155 working days from filing to decision (remarks excluded) — practice: 6–9 months, Class III up to a year, 5-year validity.
English dossier with Russian translation, Uzbek/Russian IFU, and no retail-sales license — retail runs on notification.
This guide is market-access intelligence, not regulatory or legal advice. Uzbek timelines, fees, and review practice change — professional review is required before business use.
Market Access Strategy Session
A Market Access Strategy Session maps your Uzbek route — Resolution 738 sequencing, clinical-trial and GMP readiness, and renewal planning.
Professional review is required before business use.
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