Health Canada Medical Device Reporting

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Listing Websites about Health Canada Medical Device Reporting

Incident reporting for medical devices: Guidance document

(1 days ago) Guidance documents are meant to provide assistance on howto comply with governing statutes and regulations. They also serve to … See more

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/incident-reporting-medical-devices-guidance-2021.html

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Incident reporting for medical devices : guidance document.

https://www.publications.gc.ca/site/eng/9.895027/publication.html

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Guidance document for mandatory problem reporting for …

(3 days ago) WEBCanada. Health Canada. Title : Guidance document for mandatory problem reporting for medical devices : Canada Vigilance - Medical Device Problem Reporting Program : …

https://www.publications.gc.ca/site/eng/432106/publication.html

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Report a medical device problem (for health care professionals)

(6 days ago) WEBReporting by hospitals is required Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to …

https://hpr-rps.hres.ca/side-effects-reporting-form.php?form=medical_devices

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Medical Devices Drug and Health Products Portal

(2 days ago) WEBMedical Device Incident Reports: Listing of Medical Device incidents reported to Health Canada. The incidents in this database represent the perspective of those who send …

https://dhpp.hpfb-dgpsa.ca/medical-devices

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Medical Device Incidents - Drug and Health Product Register

(9 days ago) WEBReport a medical device problem (for health care professionals) Prescription Drug List; About . Questions and Answers - Prescription Drug List; Feedback; Search Medical …

https://hpr-rps.hres.ca/mdi_landing.php

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Health Canada Adverse Event Reporting for Medical Devices

(9 days ago) WEBHere are the basic steps you should follow in reporting an adverse event in Canada: Reference Canada's Medical Device Regulations, SOR-98-282, and Guidance …

https://www.emergobyul.com/services/health-canada-adverse-event-reporting-medical-devices

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Medical Devices Regulations Summary Reports - GCcollab

(6 days ago) WEBSummary Reports –Preparation and maintenance 7 61.4 (1) The holder of a medical device licence shall prepare a summary report Who is responsible for preparing, …

https://wiki.gccollab.ca/images/9/9c/MedTech_2021_Summary_Reports_GCwiki.pdf

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Canada regulations news for medical devices and IVDs

(4 days ago) WEBThe amendments to the Medical Devices Regulations that published in the Canada Gazette, Part II (CGII) in 2020 are: The preparation, retention and submission …

https://www.medtechdive.com/spons/canada-regulations-news-for-medical-devices-and-ivds/611209/

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Serious adverse drug reactions and medical device incidents

(8 days ago) WEBMandatory reporting by hospitals. When a serious adverse drug reaction ( ADR) or medical device incident ( MDI) is documented in a hospital, the hospital must …

https://health-infobase.canada.ca/hospital-adverse-events-dashboard/

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Health Canada on Incident Reporting: Timelines and Content

(1 days ago) WEBHealth Canada, the country’s regulating authority in the sphere of medical devices, has published a guidance document dedicated to incident reporting under the …

https://www.regdesk.co/health-canada-on-incident-reporting-timelines-and-content/

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Canadian regulators issue new reporting requirements for medical …

(9 days ago) WEBDecember 5, 2021. Health Canada, the Canadian medical device market regulator, has published new guidance covering procedures and criteria for medical device …

https://www.emergobyul.com/news/canadian-regulators-issue-new-reporting-requirements-medical-device-shortages

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Health Canada Aims To Shore Up Medical Device Supply Chain …

(1 days ago) WEBCanada’s medical device regulator is seeking to protect its medical device supply chain with new reporting requirements, which came into effect on March 1 2022. …

https://www.fitchsolutions.com/bmi/medical-devices/health-canada-aims-shore-medical-device-supply-chain-new-reporting-requirements-14-03-2022

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Health Canada on Incident Reporting: Submission Content and

(9 days ago) WEBHealth Canada, the country’s regulating authority in the sphere of healthcare products, has published a guidance document dedicated to incident reporting for …

https://www.regdesk.co/health-canada-on-incident-reporting-submission-content-and-specific-aspects/

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Health Canada Guidance on Medical Device Recalls: Reporting and

(8 days ago) WEBHealth Canada, a country’s regulating authority in healthcare products, has published a guidance document dedicated to recalls. The document provides an …

https://www.regdesk.co/health-canada-guidance-on-medical-device-recalls-reporting-and-terminology/

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Recent Changes to Medical Device Regulations in Canada

(6 days ago) WEBJul 15, 2021. In last month’s #WebinarWednesday, Canadian regulatory expert Ana Subramanian discussed significant changes occurring this year with Canadian medical …

https://www.regdesk.co/summary-recent-changes-to-medical-device-regulations-in-canada/

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Consumer Medical Device Report Form - Canada

(7 days ago) WEBMedical device online voluntary reporting form for consumers, patients and general public (FRM-0317A) Skip to main content; Skip to "About government" Language selection.

https://health.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/problem-reporting/medical-device-consumer.html?wbdisable=true

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