As of today, the State Register of Medicinal Products, developed to ensure compliance with the norms outlined in the Regulation on the State Register of Medicinal Products of Ukraine, is already operating successfully.Our goal is to continuously develop and improve the functionality of the State Register of Medicinal Products. We are implementing the standards, outlined in the European Community legislation on health information systems, in Ukraine. We paid particular attention to data interoperability between various information systems.Thanks to our work, the current Ukrainian legislation is harmonized with that of the European Community, facilitating practical cooperation and data exchange between different countries.
1. Proactively involving experts.
2. Gathering requirements and turning them into a technical task for developers.
3. Designing the system from scratch with a new data model.
4. Creating a design system.
5. Ensuring oversight of the development and implementation of the best data security standards.
1. Implement preparatory measures to align the legislative framework with European legislation.
2. Integrate data on registered medicinal products into other software products, in particular, to implement the electronic stock management system for medicinal products and medical devices "eStock" (Resolution of the Cabinet of Ministers of Ukraine No. 1483 of December 30, 2022 "On the implementation of a pilot project for the implementation and operation of the electronic stock management system for medicinal products and medical devices "eStock").
3. Ensure data interoperability capabilities in the information section pertaining to the medicinal product.
4. Prepare the groundwork for mutual recognition of prescriptions within international platforms for unified information on medicinal products.
1. Ensuring compliance of the medicinal product data model in the Register with the Identification of Medicinal Products (IDMP) standards approved by the European Community legislation.
2. Ensuring that the Register’s information system is prepared for transferring information via Automated API integration.
3. Compliance of the Register’s information system with the standards of Fast Healthcare Interoperability Resources (FHIR 5.0.0).
