During a video conference held on August 11, 2026, Uzbekistan and Denmark discussed the potential for joint work in the field of pharmaceutical product regulation. This was reported by the Center for Pharmaceutical Product Safety.
Representatives from the Center for Pharmaceutical Product Safety of Uzbekistan, the Danish Medicines Agency (DKMA), and the Embassy of Uzbekistan in Sweden participated in the meeting. The Uzbek side presented information about its center's activities, its powers, and its main areas of work.
The main focus of the discussions was on state registration and inspection of medicines, pharmacovigilance, quality control of drugs, laboratory activities, ensuring the safety of pharmaceutical products, and implementing international standards.
Participants emphasized the importance of modern approaches and compliance with international norms in pharmaceutical regulation, as well as the importance of knowledge exchange and raising the professional level between regulatory bodies.
Activities of the Danish Regulator
The Danish Medicines Agency acts as the state body of Denmark responsible for regulating medicines and medical devices. Its duties include licensing and inspecting pharmaceutical companies, registering medicines, conducting clinical trials, managing pharmacovigilance, and monitoring the safety of medical devices.
Special emphasis was placed on practical ways of bilateral interaction. The parties studied possibilities for direct expert-level participation, sharing experience in regulatory practice, holding training seminars and professional development programs. The possibility of joint projects aimed at improving the qualifications of pharmaceutical industry specialists was also discussed.