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Cyprus Medical Devices Authority - ΥΠΟΥΡΓΕΙΟ ΥΓΕΙΑΣ

    https://www.moh.gov.cy/Moh/mphs/mphs.nsf/All/A82FE3D75F4BF2CAC225850A0036075A
    Cyprus Medical Devices Authority / Regulatory Information / 5. Further requirements for placing Medical Devices on Cypriot Market. Medical Devices which have already undergone the appropriate conformity assessment procedure, bearing the CE mark and registered in a EU country (or EFTA), there is no obligation for registration within the Cyprus ...

Drug & Medical Device Litigation Cyprus 2022-2023

    https://iclg.com/practice-areas/drug-and-medical-device-litigation/cyprus
    4.1 Please identify and describe the principal legislation and regulations, and any regulatory bodies, that govern the advertising, promotion and sale of drugs and …

Cyprus Medical Device Registration and Approval

    https://arazygroup.com/medical-device-registration-cyprus/
    REGULATORY AUTHORITY: Devices are regulated by the EU list of Competent Authorities.In Cyprus, devices are regulated by the Department of Medical …

Ministry of Health of the Republic of Cyprus - Legislation

    https://www.moh.gov.cy/moh/moh.nsf/legislation_en/legislation_en
    Cyprus Anti-Drugs Council. National Bioethics Committee. Cyprus Mental …

Healthcare Resource Guide: Cyprus - Trade

    https://2016.export.gov/industry/health/healthcareresourceguide/eg_main_108577.asp
    Cyprus does not have a domestic medical device manufacturing industry and all medical devices are imported. As per the Cyprus Statistical Service, imports of medical devices …

Registry of Medical Devices, State Institute for Drug Control - SUKL

    https://www.sukl.eu/medical-devices/registr-zdravotnickych-prostredku
    The State Institute for Drug Control informs on the upcoming end of the third transitional period according to Act No. 268/2014 Coll., on Medical Devices and on …

Regulatory Consulting, Cyprus, CE Marking, Medical Devices

    https://www.freyrsolutions.com/regulatory-services-in-cyprus
    Right from must-to-obtain CE marking for medical devices to successful product launch, foreign manufacturers might have to deal with the complexity of Regulatory procedures …

WEB PORTAL OF THE REPUBLIC OF CYPRUS - Laws …

    http://cyprus.gov.cy/portal/portal.nsf/gwp.getGroup?OpenForm&SectionId=government&CategoryId=Legislations&SelectionId=Laws%20regarding%20medicines&print=0&lang=en
    Laws regarding medicines. Pharmaceutical Services - European Regulations - Directives. Pharmaceutical Services - Laws - Regulatory Administrative Acts. Pharmaceutical …

European Language Translation Requirements for Medical …

    https://medenvoyglobal.com/european-language-translation-requirements-for-medical-device-labeling-ifus-and-software/
    The Medical Devices Directive (MDD) always required manufacturers to confirm whether the translation of their labeling into the national language (s) of each …

Act on Medical Devices, State Institute for Drug Control - SUKL

    https://www.sukl.eu/medical-devices/act-on-medical-devices
    Act on Medical Devices. Act No 268/2014 Coll. on Medical Devices came into effect on the First of April, 2015. This Act is a complex legal regulation which covers issue of …



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