Uzbekistan market-entry insights

Practical working notes for international companies planning an entry into Uzbekistan.

Guides

• Medical Device Registration in Uzbekistan: What Foreign Manufacturers Should Prepare Before Starting — What foreign medical device manufacturers should prepare before starting registration in Uzbekistan: authorized representative, dossier, QMS, labeling, and the recognition route under Resolution No. 738.
• Does CE Marking or FDA Clearance Replace Registration in Uzbekistan? — CE marking and FDA clearance do not replace medical device registration in Uzbekistan, but they can qualify you for a faster recognition route under Resolution No. 738. What they do — and what you still must check.
• Medical Device Registration in Uzbekistan: Documents, Participants and Typical Workflow — The document categories, the participants involved, and the typical workflow for registering a medical device in Uzbekistan under Resolution No. 738 — without pretending there is one universal document list.
• How to Find and Check a Distributor in Uzbekistan — How to find and vet a distributor in Uzbekistan: where to source candidates, the due-diligence criteria that matter, the questions to ask before signing, and the mistakes that cost foreign companies time and money.
• Entering Uzbekistan: Local Company, Distributor or Representative? — Local company, distributor or representative office — the three main ways to enter Uzbekistan compared on control, cost, speed, liability and when each fits. A practical overview, not legal advice.
• Uzbekistan Market Entry Checklist for International Companies — A practical Uzbekistan market entry checklist for international companies: company, bank account, staff, contracts, partners, tax and regulated goods — with official sources and the questions that depend on your case.