Introduction
The process of registering pharmaceutical products in Uzbekistan has changed significantly in recent years. The new rules introduced by the Ministry of Health are aimed at bringing the process closer to international standards.
Key requirements
Starting in 2024, a GMP certificate is mandatory for all imported medicines. Additional product safety reports are also required.
Required documents
- Manufacturer's license
- GMP certificate
- Product specification
- Clinical trial data (if required)
- Packaging and label samples
Process steps
- Step 1: Prepare and notarize documents
- Step 2: Submit the application to the ministry
- Step 3: Undergo the review
- Step 4: Receive the registration certificate
Conclusion
Preparing all documents in advance and working with an experienced partner is key to a successful registration. Pharm Way Group supports you at every stage of the process.
