id	domain	url
globalce-157	www.globalce.org	http://www.globalce.org
globalce-157	globalce.org	http://globalce.org
globalce-157	globalce.org	http://globalce.org
globalce-157	creativecommons.org	https://creativecommons.org/licenses/by/4.0
globalce-157	creativecommons.org	https://creativecommons.org/licenses/by/4.0
globalce-157	health.ec.europa.eu	https://health.ec.europa.eu/medical-devices-dialogue-between-interested-parties/overview_en#competent-authorities-for-medical-devices---camd
globalce-157	health.ec.europa.eu	https://health.ec.europa.eu/medical-devices-dialogue-between-interested-parties/overview_en#competent-authorities-for-medical-devices---camd
globalce-157	ec.europa.eu	https://ec.europa.eu/docsroom/documents/32305
globalce-157	ec.europa.eu	https://ec.europa.eu/docsroom/documents/32305
globalce-157	www.ecfr.gov	https://www.ecfr.gov/current/title-21/chapter-i/subchapter-a/part-7
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities
globalce-157	www.ecfr.gov	https://www.ecfr.gov/current/title-21/chapter-i/subchapter-a/part-7
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude
globalce-157	www.ecfr.gov	https://www.ecfr.gov/current/title-21/chapter-i/subchapter-h/part-803
globalce-157	www.ecfr.gov	https://www.ecfr.gov/current/title-21/chapter-i/subchapter-h/part-803
globalce-157	ncrdscb.ada.org	https://ncrdscb.ada.org/recognized-dental-specialties
globalce-157	ncrdscb.ada.org	https://ncrdscb.ada.org/recognized-dental-specialties
globalce-157	link.springer.com	https://link.springer.com
globalce-157	www.fda.gov	https://www.fda.gov
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices
globalce-157	ec.europa.eu	https://ec.europa.eu
globalce-157	www.tga.gov	https://www.tga.gov
globalce-157	link.springer.com	https://link.springer.com/chapter/10.1007/978-3-319-74098-0_8
globalce-157	link.springer.com	https://link.springer.com/chapter/10.1007/978-3-319-74098-0_8
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/about-manufacturer-and-user-facility-device-experience-maude
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems
globalce-157	ec.europa.eu	https://ec.europa.eu/tools/eudamed/#/screen/home
globalce-157	ec.europa.eu	https://ec.europa.eu/tools/eudamed/#/screen/home
globalce-157	www.tga.gov.au	https://www.tga.gov.au/safety/safety/safety-monitoring-medical-devices
globalce-157	www.tga.gov.au	https://www.tga.gov.au/safety/safety/safety-monitoring-medical-devices
globalce-157	www.gov.uk	https://www.gov.uk/drug-device-alerts
globalce-157	www.bfarm.de	https://www.bfarm.de/en/medicaldevices/tasks/risk-assessment-and-research/fieldcorrective-actions/_node.html
globalce-157	www.drugwatch.com	https://www.drugwatch.com
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/infusion-pumps
globalce-157	canada.ca	http://canada.ca
globalce-157	recalls-rappels.canada.ca	https://recalls-rappels.canada.ca/en
globalce-157	recalls-rappels.canada.ca	https://recalls-rappels.canada.ca/en
globalce-157	mhra.gov.uk	http://mhra.gov.uk
globalce-157	www.gov.uk	https://www.gov.uk/drug-device-alerts
globalce-157	www.bfarm.de	https://www.bfarm.de/en/medical-devices/tasks/risk-assessment-and-research/field-corrective-actions/_node.html
globalce-157	www.bfarm.de	https://www.bfarm.de/en/medical-devices/tasks/risk-assessment-and-research/field-corrective-actions/_node.html
globalce-157	www.bfarm.de	https://www.bfarm.de/en/medical-devices/tasks/risk-assessment-and-research/field-corrective-actions/_node.html
globalce-157	drugwatch.com	http://drugwatch.com
globalce-157	www.drugwatch.com	https://www.drugwatch.com/hip-replacement/recalls
globalce-157	www.drugwatch.com	https://www.drugwatch.com/hip-replacement/recalls
globalce-157	www.federalregister.gov	https://www.federalregister.gov/documents/2014/02/14/2014-03279/medical-device-reporting-electronic-submission-requirements
globalce-157	www.federalregister.gov	https://www.federalregister.gov/documents/2014/02/14/2014-03279/medical-device-reporting-electronic-submission-requirements
globalce-157	www.federalregister.gov	https://www.federalregister.gov/documents/2014/02/14/2014-03279/medical-device-reporting-electronic-submission-requirements
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/infusion-pumps/examples-reported-infusion-pump-problems
globalce-157	www.fda.gov	https://www.fda.gov/medical-devices/infusion-pumps/examples-reported-infusion-pump-problems