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EUR-Lex - 32016L0097 - EN - EUR-Lex - Europa

    https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32016L0097
    Insurance and reinsurance intermediaries shall hold professional indemnity insurance covering the whole territory of the Union or some other comparable guarantee against liability arising from professional negligence, for at least EUR 1 250 000 applying …

EUR-Lex - 32009L0138 - EN - EUR-Lex - Europa

    https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32009L0138
    Council Directive 64/225/EEC of 25 February 1964 on the abolition of restrictions on freedom of establishment and freedom to provide services in respect of reinsurance and …

Insurance Distribution Directive (IDD) | Eiopa - Europa

    https://www.eiopa.europa.eu/browse/regulation-and-policy/insurance-distribution-directive-idd_en

    Public health support – EU action

      https://european-union.europa.eu/priorities-and-actions/actions-topic/health_en
      In addition to formulating EU-wide laws and standards for health products and services, it also provides funding for health projects across the EU. Summaries of EU legislation on health; EU health …

    The European directive on patients' rights - Cleiss

      https://www.cleiss.fr/docs/directive_en.html
      Content of the directive The Directive aims to facilitate access to safe, high-quality cross-border healthcare and to promote healthcare-related cooperation between …

    Cross-Border Healthcare Directive - Citizens Information

      https://www.citizensinformation.ie/en/health/eu_healthcare/cross_border_directive.html
      Cross-Border Healthcare Directive If you are entitled to public health services in Ireland, you may opt to access those services in another member state of the European Union or …

    Medical devices | European Medicines Agency

      https://www.ema.europa.eu/en/human-regulatory/overview/medical-devices
      The Medical Devices Regulation applies since 26 May 2021. Manufacturers must comply with the Regulation when placing new medical devices on the market. It …

    Clinical Trials Regulation | European Medicines Agency

      https://www.ema.europa.eu/en/human-regulatory/research-development/clinical-trials/clinical-trials-regulation
      European Union (EU) pharmaceutical legislation known as the Clinical Trials Regulation entered into application on 31 January 2022. It aims to ensure the EU …

    The European Union Medical Device Regulation – …

      https://eumdr.com/
      Press release 26 May 2021: announcing Stronger rules on medical devices (EU MDR) have entered into application. Publication of MDCG 2021-8 Clinical investigation …

    Directives - Public Health

      https://health.ec.europa.eu/medical-devices-sector/directives_en
      Market Surveillance and Vigilance The Medical Devices Directives establish specific procedures that national authorities must follow when considering the enforcement of the …



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