The Ministry of Health of Ukraine approved guidelines that are developed on the basis of relevant documents of the European Commission (MEDDEV) for an unambiguous interpretation of technical regulations regarding medical devices, medical devices for in vitro diagnostics and active implantable medical devices.
The recommendations are not legally binding, but should be taken into account by manufacturers, authorized representatives, conformity assessment bodies and state market surveillance authorities, and other medical device market operators.
Download guidelines here
Text is available only in Ukrainian
Read moreText is available only in Ukrainian
Read moreThe American Chamber of Commerce in Ukraine, jointly with the member company UNI-CERT LLC, is glad to invite you to the upcoming Knowledge Webinar “Recognition of CE Certificates for Medical Devices in 2023: What You Need to Know?” scheduled for Tuesday, October 17, 11:00 AM. Don’t miss an exceptional opportunity to learn from speakers on the main principles of […]
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