FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI DAVLAT MUASSASASI

Company Introduction:

Location: Uzbekistan

Type of Entity:

This organization is neither a factory (manufacturer) nor a trading company. It is a state institution, functioning as a regulatory and quality control body for pharmaceutical products and medical devices in Uzbekistan.

Company Overview:

The State Institution "Center for Pharmaceutical Product Safety" is the primary governmental body in Uzbekistan responsible for ensuring the quality, safety, and efficacy of pharmaceutical products and medical devices circulating within the country. Its core functions include:

1. Quality Control and Expertise: Conducting laboratory analyses and expert evaluations of medicines, medical devices, and other pharmaceutical products.

2. Standardization and Certification: Developing and implementing national standards for pharmaceutical products and issuing certificates of conformity.

3. Registration and Licensing Support: Participating in the processes of state registration and licensing of pharmaceutical activities.

4. Pharmacovigilance: Monitoring the safety of medicines after their introduction to the market, including adverse event reporting.

5. Regulatory Oversight: Contributing to the development and enforcement of legislation related to pharmaceutical circulation.

The institution plays a crucial role in protecting public health by ensuring that only safe, high-quality, and effective pharmaceutical products are available to the population of Uzbekistan.

The State Institution Center for Safety of Pharmaceutical Products (FARMATSEVTIKA MAHSULOTLARI XAVFSIZLIGI MARKAZI DAVLAT MUASSASASI) in Uzbekistan does not manufacture or sell any products.

This institution functions as a regulatory and quality control body. Its primary role is to ensure the safety, quality, and efficacy of pharmaceutical products and medical devices available in the Republic of Uzbekistan. Its key activities related to products include:

State registration and certification of medicines and medical devices.

Conducting laboratory testing and analysis of pharmaceutical products for quality control.

Monitoring and evaluating adverse drug reactions (pharmacovigilance).

Issuing permits related to the import and export of pharmaceutical products.

Developing and enforcing standards and regulations for the pharmaceutical industry.