1. Issues and challenges in the registration and certification of medicinal products, and the review of these processes. Ensuring support from European Union diplomatic missions in organizing the exchange of experience between leading EU experts in drug registration and relevant organizations and specialists in Uzbekistan.
2. Collaboration between the Committee and state organizations and regulatory bodies of Uzbekistan in establishing a pharmacovigilance system for medicinal products that meets international standards. Ensuring support from European Union diplomatic missions in organizing the exchange of experience between leading EU experts in pharmacovigilance and relevant organizations and specialists in Uzbekistan.
3. Proposals to complete the process of deregulating drug prices, at least at the retail level.
4. Intellectual property issues, including parallel importation and the similarity of local product trademarks.
5. Discussion of the list of European countries whose manufacturers are exempt from undergoing pharmaceutical inspections by Uzbekistan's state authorities for the purpose of drug registration.
6. Development of health insurance and its future prospects.
7. Identifying prospective areas of collaboration in the life sciences between the Committee and Uzbekistan's Ministry of Health.