The meeting was devoted to discussion of:
- Working Group’s activities in Q1
- Updates on harmonization of Technical Regulations for medical devices and in vitro diagnostic medical devices with corresponding regulations in the European Union
- Status of PCR testing of donated blood in 2025, including the timely preparation and submission of technical specifications for the centralized procurement of reagents, consolidated demand from blood system entities, and remaining stocks of test kits
- Legal aspects of the recognition of EU certificates for medical devices in Ukraine
- Establishment of the Ukrainian Pharmaceutical Agency with regard to the regulation and management of medical devices
- State diagnostic and screening programs
Contacts
