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PHARMALEXREGULATORY AFFAIRS · UZBEKISTAN

Medicine registrationNew medicines, generics and biologics: from dossier to certificate.
Medical device registrationDevices of every risk class: technical file, testing, expert review.
Medical equipment registrationEquipment for clinics and laboratories, including service documents.
Re-registrationWe renew the registration before the certificate expires.
VariationsA new manufacturer, pack, composition or patient leaflet.
Dietary supplement registrationImport and production permit, sanitary-epidemiological conclusion.

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PHARMALEXREGULATORY AFFAIRS · UZBEKISTAN

Pharmalex registers medicines, medical devices and equipment, and dietary supplements in Uzbekistan for foreign manufacturers and importers.

PHARMALEX Private Enterprise7a/31 Yangi Olmazor Street, Almazar District, Tashkent 100000, Uzbekistan+998 94 050 66 88 info@pharmalex.uz

© Pharmalex

Services

Medicine registration Medical device registration Medical equipment registration Re-registration Variations Dietary supplement registration

Company

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MedicinesNeeds review

National Good Manufacturing Practice standard — Center source

The Center index lists a GMP standard identified as O`zDSt 2766:2018. Its applicable version and relationship to earlier standards are not confirmed.

Act type: State standard
Section: Quality, GxP and pharmacopoeia

Official text

National Good Manufacturing Practice standard — Center source

State standard

Open on uzpharm-control.uz

GMP standards
source requires review

Official sources

Indexed attachment — content unreviewed

Related documents

Cabinet of Ministers Resolution · No. 472 · 7 September 2026Checked against the official sourceOn additional measures to improve legislation on technical regulationMedicines
Order of the Minister of Health · No. 14 · 10 April 2026Checked against the official sourceProcedure for setting fees for GxP pharmaceutical inspection of pharmaceutical enterprises and preclinical and clinical research sitesMedicinesMedical devices and equipment
Order of the Minister of Health · No. 13 · 16 December 2025Checked against the official sourceCertification-rule amendments covering GMP and ISO 13485 — No. 3386-2MedicinesMedical devices and equipment
Order of the Minister of Health · No. 14 · 12 December 2025Checked against the official sourceDevelopment and inclusion of general and individual pharmacopoeial monographsMedicines