Your Trusted Partner for Pharmacovigilance Support in Uzbekistan
Uzbekistan is emerging as a key pharmaceutical market in Central Asia, driven by healthcare reforms, regulatory modernization, and increased focus on drug safety and post-marketing surveillance. As the country strengthens its pharmacovigilance framework, pharmaceutical companies must establish locally compliant safety systems supported by strong regulatory coordination.
Market success in Uzbekistan depends not only on product registration but also on continuous pharmacovigilance compliance, local accountability, and timely safety reporting.
At DDReg, we provide end-to-end pharmacovigilance services in Uzbekistan, helping companies ensure compliance, mitigate risk, and maintain patient safety across the product lifecycle.
Pharmacovigilance Framework in Uzbekistan
Pharmacovigilance in Uzbekistan is regulated by the Center for Pharmaceutical Products Safety under the Ministry of Health.
The authority is responsible for:
- Monitoring adverse drug reactions (ADRs)
- Ensuring post-marketing safety surveillance
- Enforcing pharmacovigilance compliance
- Supporting public health protection through risk minimization
Uzbekistan’s regulatory system is evolving, with increasing emphasis on structured pharmacovigilance systems and local regulatory engagement.
Normative Framework Governing Pharmacovigilance in Uzbekistan
Pharmacovigilance obligations in Uzbekistan are defined through national regulatory instruments:
- Order No. 13 of the Minister of Health (March 9, 2018) – Core guideline outlining pharmacovigilance requirements, responsibilities, and reporting obligations
- Ministry of Health Regulations – Additional directives governing drug safety monitoring and compliance
These frameworks require companies to maintain robust safety systems and proactive regulatory communication.
Local Pharmacovigilance Requirements in Uzbekistan
Uzbekistan places strong emphasis on local pharmacovigilance responsibility and in-country regulatory coordination.
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Key Requirement: Local Pharmacovigilance Contact
- Mandatory for all Marketing Authorization Holders (MAHs)
- Must be based in Uzbekistan
- Must be appropriately qualified and experienced in pharmacovigilance
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Responsibilities of the Local PV Contact
- Management of adverse event (AE) reporting
- Implementation of pharmacovigilance activities
- Coordination with the Ministry of Health and regulatory authority
- Ensuring compliance with national pharmacovigilance requirements
This makes local presence essential for maintaining compliance in Uzbekistan.
DDReg provides comprehensive drug safety services in Uzbekistan, ensuring compliance with national regulations and global pharmacovigilance standards.
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Individual Case Safety Report (ICSR) Management
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Aggregate Reporting & Safety Writing
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Signal Detection & Risk Management
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Local Pharmacovigilance Compliance in Uzbekistan
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Literature Screening & Safety Intelligence
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Pharmacovigilance Consulting Services in Uzbekistan
Why Choose DDReg as Your Pharmacovigilance Company in Uzbekistan?
Strong understanding of Uzbekistan’s pharmacovigilance framework and compliance expectations.
End-to-End Drug Safety ServicesSupport across clinical and post-marketing phases.
Compliance-Driven ApproachEnsuring adherence to national regulations and global best practices.
Inspection-Ready SystemsPrepared for audits and regulatory inspections.
Scalable SolutionsFlexible models designed for growing pharmaceutical portfolios.
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