Registration & Certification
End-to-end support for registration of medical devices, medicines and supplements in Uzbekistan: documentation, expertise, regulator communication.
Medical Devices
Registration, dossier, support
Medicines / Supplements
Documents, expertise, submission
Your product. Our paperwork
Who we help
Manufacturers, importers, laboratories, clinics — any business that needs registration in Uzbekistan.
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Manufacturers
Document package, test and expert review support.
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Importers
Fast market entry and reduced rejection risk.
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Laboratories
Certification works, test plans and protocols.
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Clinics
Documentation and compliance assessment, consultations.
Services
Turnkey or specific tasks. Tailored to your product.
Medical Device Registration
Classification, dossier, regulator interaction.
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Medicine Registration
Document preparation, expert review support.
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Supplement Registration
Document package and requirements consulting.
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Certification / ISO
Organizing certification works and audits.
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Expert Conclusions
Documentation audit and compliance strategy.
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FAQ
Short and to the point. We'll discuss the rest during the work.
Depends on product category, dossier completeness and regulator requirements. We first assess documents, then give a realistic plan.
Yes. We can start with an audit of existing documents: what's there, what's missing, what's critical, what can be submitted later.
Base is Uzbekistan. If needed, we can help prepare packages for other markets (FDA, PMDA, NMPA, EC, Russia).
Latest articles
Reference pages on Uzbekistan regulatory affairs.
Uzbekistan
How to prepare a medical device dossier
Step-by-step structure: what is mandatory, what is often forgotten.
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Practice
Typical reasons for rejections
How to preemptively address document and labeling risks.
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ISO
What ISO 13485 really gives you
When ISO is needed, when it's unnecessary, and how to avoid overpaying.
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