Health Care

13/ 08/ 2021

On August 13, 2021, the Head and the Manager of the Medical Devices Subcommittee met with the leaders and experts of the State Expert Center of the MOH of Ukraine on developing the Guideline for the Health Technology Assessment for Medical Devices (HTA MD). During the meeting, participants discussed the plan for the Guidelines development, the status of its readiness as of today, the main articles, the definition of clear criteria for the medical devices classification, and the medical devices category that can be a subject for OMT. After the approval of the HTA MD Guideline, all companies that are planning to participate in public procurement will be required to go through the OMT procedure. We are planning to hold such meetings on the regular basis.

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During the meeting, participants discussed the plan for the Guidelines development, the status of its readiness as of today, the main articles, the definition of clear criteria for the medical devices classification, and the medical devices category that can be a subject for OMT. After the approval of the HTA MD Guideline, all companies that are planning to participate in public procurement will be required to go through the OMT procedure. We are planning to hold such meetings on the regular basis.