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Read moreOn January 6, 2023 the European Commission adopted a proposal to give more time to certify medical devices to mitigate the risk of shortages. The proposal introduces a longer transition period to adapt to new rules, as foreseen under the Medical Devices Regulation. The new deadlines depend on the medical devices’ risk class and will […]
Read moreOn August 31, the 12th Ukrainian Forum of Medical Devices Market Operators was held, which provided manufacturers, suppliers, distributors, and importers of medical devices with a platform for solving all urgent issues, discussions, recommendations, and sharing valuable experience in doing business during martial law. The Ukrainian Scientific Institute of Certification traditionally sponsored this event. In […]
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