OF MEDICINES IN
THE REPUBLIC OF UZBEKISTAN
THE REPUBLIC OF UZBEKISTAN
REGISTRATION OF MEDICINES IN THE REPUBLIC OF UZBEKISTAN
Planning to launch a medicinal product on the market of the Republic of Uzbekistan?
You’ve come to the right place. Registrarius Pharm Expert will guide your product through the entire regulatory pathway – from registration dossier preparation to obtaining the marketing authorization. We structure the process to minimize deficiencies, rework and delays.
With over 20 years of experience, we have completed more than 2,000 successful registrations of medicines, medical devices, food supplements, cosmetics, and food products in the territory of the countries.
Free initial consultation and cost estimate – we will answer all your questions and calculate the project budget through any communication channel convenient for you
You’ve come to the right place. Registrarius Pharm Expert will guide your product through the entire regulatory pathway – from registration dossier preparation to obtaining the marketing authorization. We structure the process to minimize deficiencies, rework and delays.
With over 20 years of experience, we have completed more than 2,000 successful registrations of medicines, medical devices, food supplements, cosmetics, and food products in the territory of the countries.
Free initial consultation and cost estimate – we will answer all your questions and calculate the project budget through any communication channel convenient for you
Gaukhar Bilimbayeva, CEO of Registrarius Pharm Expert LLP, PharmD, MBA
Upon receipt of your request, we will prepare a personalized commercial proposal with a detailed calculation of the full budget for the registration of your product in the Republic of Uzbekistan. No hidden fees – you see the final price before the contract is signed.
PARTNERSHIP MODEL WITH REGISTRARIUS PHARM EXPERT
COMMERCIAL PROPOSAL
[01]
Bilimbayev Dauren,
Founder of Registrarius Pharm Expert
Founder of Registrarius Pharm Expert
We sign an official contract with clearly defined timelines, obligations of the parties, and payment procedure. Payment is made in accordance with the terms of the agreement – flexibly and conveniently for your accounting department.
CONTRACT AND PAYMENT
[02]
Registrarius Pharm Expert manages the project from kick-off to handover to the Client in full compliance with the contract terms. You receive regular progress reports on the registration, prompt feedback, and support at every stage of interaction with the Authority.
PROJECT EXECUTION
[03]
FROM 1 TO 12 MONTHS
Preparation of the registration dossier, reference standards and samples
UP TO 30 DAYS
Submission of the dossier for registration
FROM 210 TO 345 DAYS
Examination procedure and issuance of the marketing authorization
Planning to launch a medicinal product on the pharmaceutical market of the Republic of Uzbekistan? We have prepared for you a clear breakdown of all stages of state registration.
Our experience in the registration of medicines in the CIS countries is backed by proven procedures and realistic timelines. Only working solutions, no inflated promises.
Our experience in the registration of medicines in the CIS countries is backed by proven procedures and realistic timelines. Only working solutions, no inflated promises.
STATE REGISTRATION PROCESS FOR MEDICINES
1.1
2.1
RECEIPT OF THE DOSSIER, REFERENCE STANDARDS AND SAMPLES FROM THE MANUFACTURER
EXAMINATION AND REGISTRATION PROCEDURE
At this sub-stage, the basis for the state registration of the product is formed: the registration dossier is collected
Timelines depend directly on how quickly the manufacturer provides the complete package of documents, reference standards and samples, and we, in turn, shorten them by giving the manufacturing site precise and clear requirements from the outset.
Timelines depend directly on how quickly the manufacturer provides the complete package of documents, reference standards and samples, and we, in turn, shorten them by giving the manufacturing site precise and clear requirements from the outset.
The most critical stage. Experts of the Center for Pharmaceutical Product Safety carry out a comprehensive review of the product dossier and samples The examination takes place in several stages: primary examination (verification of the completeness, integrity and correct formatting of the dossier), laboratory testing of samples (confirmation of the reproducibility of the analytical methods specified in the Normative Document) and specialized examination (pharmaceutical and pharmacological assessment of safety, efficacy and quality, as well as of the compliance of the instructions for use, SmPC, Normative Document, labeling and packaging with the requirements of Uzbekistan). At each stage, the experts may issue deficiency letters, and the speed and quality of the responses determine the overall registration timeline. Our specialists promptly address all queries and deficiencies to minimize clock-stops and avoid delays in obtaining the marketing authorization.
1.2
2.2
ADAPTATION OF DOCUMENTS TO THE REQUIREMENTS OF UZBEKISTAN
ISSUANCE OF THE MARKETING AUTHORIZATION
In parallel, our team prepares a package of documents adapted to the requirements of the Center for Pharmaceutical Product Safety:
The final stage – the application and the examination materials are submitted for review to the Presidium of the Authority, where conformity with the expert report is re-verified. Upon a positive decision of the Presidium, the applicant is issued a marketing authorization valid for 5 years, which confirms the safety, efficacy and quality of the product and grants the right to import and market it in the territory of the Republic of Uzbekistan. The product data are entered in the State Register of Medicines.
- Translation of the instructions for medical use and packaging mock-ups into the state language
- Development of the local SmPC and the Normative Quality Document
- Notarization of dossier sections and preparation of the application for state registration
Stage #I
Each of the above stages has its own processes, timelines, nuances and risks, which we will help you successfully overcome with maximum benefit for you!!! Each of the above stages has its own processes, timelines, nuances and risks, which we will help you successfully overcome with maximum benefit for you!!! Each of the above stages has its own processes, timelines, nuances and risks, which we will help you successfully overcome with maximum benefit for you!!!
1–12 months
210 days
up to 30 days
up to 15 days
Preparation of the dossier, reference standards and samples
Duration – from 1 to 12 months
Duration – from 1 to 12 months
Stage #II
Submission of the dossier and samples, examination and registration
Duration – up to 1 month for submission and payment of the examination fee, 210 days for examination and registration / 7 months*
*excluding clock-stops (time for addressing deficiency letters).
Including clock-stops – up to 345 days / 12 months
Duration – up to 1 month for submission and payment of the examination fee, 210 days for examination and registration / 7 months*
*excluding clock-stops (time for addressing deficiency letters).
Including clock-stops – up to 345 days / 12 months
The foundation of the registration procedure. Many of the deficiencies that cause the examination to drag on for months originate right here, before submission. We know which nuances are critical for the experts of the Authority, and we build the dossier so that as few questions as possible arise during the examination.
Once the dossier is fully assembled, the documents, reference standards and samples are officially submitted to the Authority, and the examination procedure established by the legislation of the Republic of Uzbekistan begins.
You don't need to figure out the national specifics – that is our area of responsibility. The timeline can be shortened if the manufacturer provides source materials in advance.
Common registration risks
and ways to overcome them
and ways to overcome them
Discrepancies between the CPP or the marketing authorization and the documents of the registration dossier
Advance verification and elimination of inconsistencies and discrepancies before submitting documents to the Center for Pharmaceutical Product Safety.
Absence of a valid GMP certificate for the manufacturing site
Checking the validity of the GMP certificate and arranging a re-inspection, if necessary, before the procedure begins.
Non-compliance of analytical methods and quality standards with the requirements of Uzbekistan
Preliminary review of the product's regulatory documentation for compliance with local requirements and development of the Normative Document before the official submission.
Late provision of samples or responses to expert queries by the manufacturer
Informing the manufacturer about possible queries at the dossier preparation stage and monitoring of timelines.
Integrity and reputation are the foundation of our business.
We work so that, after the project is completed, you will want to recommend us to colleagues and partners. Every marketing authorization, every completed stage, is a contribution to the Company name we build painstakingly and meticulously, year after year.
The cost of a mistake is months of lost time and a derailed product launch. We understand this and therefore work with full responsibility for every stage and every document.
Deception, failure to deliver, or shifting responsibility are absolutely unacceptable to us. We take on a project only when we are confident that we will see it through to a successful outcome in the shortest possible timeframe.
We work so that, after the project is completed, you will want to recommend us to colleagues and partners. Every marketing authorization, every completed stage, is a contribution to the Company name we build painstakingly and meticulously, year after year.
The cost of a mistake is months of lost time and a derailed product launch. We understand this and therefore work with full responsibility for every stage and every document.
Deception, failure to deliver, or shifting responsibility are absolutely unacceptable to us. We take on a project only when we are confident that we will see it through to a successful outcome in the shortest possible timeframe.
A RELIABLE PARTNER IN MEDICINES REGISTRATION IN UZBEKISTAN
Our guarantee
Registrarius Pharm Expert is built upon the professional expertise of one of its founders and the CEO of the company – Gaukhar Bilimbayeva,
120 years of combined team experience, GMP inspections and audits
Over these years, we have progressed from registering straightforward generics to complex cases involving biological products, medical devices and non-standard manufacturing sites. This experience is your insurance against delays, refusals and rework
120 years of combined team experience, GMP inspections and audits
Over these years, we have progressed from registering straightforward generics to complex cases involving biological products, medical devices and non-standard manufacturing sites. This experience is your insurance against delays, refusals and rework
Company experience
successful GMP inspections by the Authorities of the CIS
more than 2,000 successful regulatory approvals, including medicines, medical devices, food supplements, cosmetics, and food products; we have organized and supported inspections and audits:
More than 30
successful internal audits with a positive GXP, GRP and GVP conclusion
More than 50
successful quality control inspections
More than 10
Our track record
Maxim Sevostyanov
Director of Global Regulatory and Medical Translations
Education:
2015—2019 — Manash Kozybayev
North Kazakhstan University
gaukhar bilimbayeva
Chief Executive Officer (CEO), PharmD, MBA
Education:
1997—2002 — S. Asfendiyarov Kazakh National Medical University
2016—2018 — MBA, Swiss Business School, Zurich, Switzerland
dauren bilimbayev
Founder
Education:
2000—2004 — T. Ryskulov Kazakh Economic University
2003—2005 — S. Amanzholov East Kazakhstan State University
2016—2017 — NIMA International Marketing School, the Netherlands
Anna polivoda
Deputy CEO, Head
of Sales and Marketing
Education:
2018—2022 — Almaty Management University (AlmaU)
2022—2024 — Sh. Murtaza International University
gulzhan akhmetova
Head of Registration Department,
Quality Responsible Person
Education:
2005—2009 — Al-Farabi Kazakh National University
2013—2015 — K. I. Satpayev Kazakh National Technical University (KazNTU)
Bulegenova Zhadyra
Senior Registration Specialist
Education:
2008-2012 — Al-Farabi Kazakh National University (Bachelor's)
2012-2014 — S. Asfendiyarov Kazakh National Medical University (Master's)
Jenis Kamila
Registration Specialist
Education:
2016-2020 — S. Asfendiyarov Kazakh National Medical University
Asel Seidakhmetova
Senior Registration Specialist
Education:
2006-2010 — Kazakh National Agrarian University (KazNAU)
Client testimonials
Client testimonials
Frequently asked questions about the registration of medicines in Uzbekistan
How long does it take to register a medicinal product in Uzbekistan?
Preparation of the dossier, reference standards and samples takes from 1 to 12 months. This is followed by up to 1 month for submission and payment of the examination fee and 210 days for examination and registration, excluding clock-stops; including clock-stops, the timeline is up to 345 days.
Which authority carries out the examination of medicines in Uzbekistan?
The dossier and samples are examined by experts of the Center for Pharmaceutical Product Safety. The examination includes a primary examination, laboratory testing of samples and a specialized examination (pharmaceutical and pharmacological assessment).
For what period is a marketing authorization for a medicine issued in Uzbekistan?
The application and examination materials are reviewed by the Presidium of the authority. Upon a positive decision, a marketing authorization valid for 5 years is issued, and the product data are entered in the State Register of Medicines.
Which documents need to be adapted to the requirements of Uzbekistan when registering a product?
The instructions for medical use and packaging mock-ups are translated into the state language, a local SmPC and Normative Quality Document are developed, dossier sections are certified, and the application for state registration is prepared.
Which risks most often delay the registration of a medicine in Uzbekistan?
Common risks include discrepancies between the CPP or marketing authorization and the dossier documents, the absence of a valid GMP certificate for the site, and non-compliance of analytical methods with the requirements of Uzbekistan. These points are checked before the documents are submitted.
REGISTRARIUS PHARM EXPERT office in Uzbekistan
REGISTRARIUS PHARM EXPERT office in Kazakhstan
Republic of Kazakhstan, Almaty 050000
Miras microdistrict, Tan Nury residential complex, 128, apartment 19
Sales hotline: +7 (700) 178-67-67
Mail: info@registrarius.org
Miras microdistrict, Tan Nury residential complex, 128, apartment 19
Sales hotline: +7 (700) 178-67-67
Mail: info@registrarius.org
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Guaranteed deadlines
Planning negotiations.
Contract signing
Contract signing
Handover. Project launch
Monthly reports.
Online tracking
of product statuses.
Participation in reporting meetings
Online tracking
of product statuses.
Participation in reporting meetings
Cost savings
More time for business
Lower taxes
Freeing up a staff position
Qualified managers
Focus on your business, while we take care of registration and pharmacovigilance!
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