News

08.02.2024

Post-marketing surveillance. A framework for studying, analyzing and preventing adverse events associated with medical devices on the market.

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23.01.2024

Risk management, the basis of integrated management

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15.01.2024

Legislation of Ukraine in the field of technical regulation of medical devices

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03.01.2024

EU certificate for medical devices: the thorny path of recognition

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13.12.2023

Natal chart of a medical device: how is the MD class determined?

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27.11.2023

Contract manufacturing: requirements are becoming more stringent

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