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BfArM - Public databases

    https://www.bfarm.de/EN/Medical-devices/Tasks/DMIDS/Public-databases/_node.html
    Licensing. Types of Marketing Authorisation; Licensing Procedures; Follow-up Procedures; Issues Relevant for Licensing; Medicines for children; Medicines for rare diseases; Pharmacovigilance. Reporting risks; Risk information; Periodic Safety Update Reports …

Germany Medical Device Registration - BfArM and …

    https://arazygroup.com/medical-device-registration-germany/
    In Germany, devices are regulated by the The Federal Institute for Drugs and Medical Devices (BfArM) and The German Institute of Medical Documentation and …

Q&A: pharma & medical device regulation in Germany

    https://www.lexology.com/library/detail.aspx?g=4e521a96-5e31-43f8-a45e-e4d080d32452
    Germany December 10 2019 Health services framework and competent authorities Healthcare bodies Describe the bodies and their responsibilities (public and …

Medical Device Registration in Germany - Thema Med

    https://www.thema-med.com/en/medical-device-registration-in-germany/
    Medical Device Registration in Germany. All Medical Devices must bear the CE marking in order to be marketed. Non-EU Manufacturers must appoint an Authorized European …

Medical Device Regulations in Germany

    https://www.regdesk.co/reg-ger/
    Since Germany is a European Union member country, it follows the device classification system that of …

BfArM - Medical devices - Import to Germany

    https://www.bfarm.de/EN/Medical-devices/_FAQ/DMIDS-import/faq-liste.html
    There is a possibility of registering "importers" in the sense of the German Medical Devices Act (MPG), however, we want to point out the definition in § 5 MPG. It is stated there that …

Germany - Healthcare and Medical Technology

    https://www.trade.gov/country-commercial-guides/germany-healthcare-and-medical-technology
    Germany claims the third-largest medical technology market in the world after the United States and Japan and is by far the largest European market, twice the size of …

Medical device registration Germany, Notification, …

    https://medicaldevices.freyrsolutions.com/medical-devices-regulatory-services-germany
    Medical device registration Germany, Notification, classification, BfArM, DIMDI Germany Regionwide Expertise Contact Us +1 908 483 7958 [email protected]

Regulatory and Start-up Guideline for Clinical Trials …

    https://www.germannetpaet.de/fileadmin/Media/06_Material/Regulatory_and_Start-up_Guideline_Clinical_Trials_Germany_final_2019.pdf
    German Narcotic Drugs Act Chemistry, Manufacturing and Control Clinical Trial Application for the Authorisation of Clinical Trials Clinical Trial Regulation Ethics Committee for …

Licensing International Germany | Licensing International

    https://licensinginternational.org/germany/
    Licensing International Germany | Licensing International Directory Events Membership Careers About Education News Data Sign Up for Updates Für unsere Mitglieder Der Tag …



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