Health Canada Incident Reporting

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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.

(5 days ago) WEBCanada. Health Canada, issuing body. Title : Incident reporting for medical devices : guidance document. Publication type : Monograph : Language [English] Other language …

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

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Medical Device Incidents - Drug and Health Product Register

(9 days ago) WEBSubmit a report . Report a side effect; Report a serious adverse drug reaction (for hospitals) Report a medical device problem (for health care professionals) Prescription …

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

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Health Canada on Incident Reporting: Timelines and …

(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 new regulatory framework, which …

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

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Industry Medical Device Report Form - Canada.ca

(7 days ago) WEBDetails on personal information collected under this program are outlined on the Info Sources Web site and are described in the Health Canada section (see Personal …

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

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Guidance on Mandatory Incident Reporting under the Canada …

(2 days ago) WEBBy law, companies must inform Health Canada within two days of becoming aware of a health or safety incident related to a consumer product they manufacture, import, or …

https://cscb.ca/article/guidance-mandatory-incident-reporting-under-canada-consumer-product-safety-act

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Side Effect Reporting - Drug Health Product Register

(6 days ago) WEBA. Report and submitter information. Type of report: Indicate whether the report is the first one submitted for this specific medical device incident (i.e. initial) or a follow-up to a …

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

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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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The Canadian Medication Incident Reporting and Prevention System

(6 days ago) WEBThe Canadian Medication Incident Reporting and Prevention System (CMIRPS) is a collaborative pan-Canadian program of Health Canada, the Canadian Institute for …

https://www.cmirps-scdpim.ca/?p=14&lang=en

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CMIRPS - ISMP Canada

(Just Now) WEBThe Canadian Medication Incident Reporting and Prevention System (CMIRPS) is a collaborative pan-Canadian program of Health Canada, ISMP Canada, Canadian …

https://ismpcanada.ca/impact/canadian-medication-incident-reporting-and-prevention-system/

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Health Canada Guidance on Incident Reporting RegDesk

(6 days ago) WEBMar 20, 2021. Health Canada, the country’s regulating authority in the sphere of medical devices, has published updated guidance on incident reporting for medical devices. …

https://www.regdesk.co/health-canada-incident-reporting/

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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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Guidelines for Safety Reporting Requirements to Health …

(6 days ago) WEBThis includes cases in which the incident: *The preliminary report shall be submitted: • Within 10 days after the manufacturer or importer of a medical device becomes aware of …

https://wprod.sickkids.ca/siteassets/research/reb/research-ethics-guidelines/sickkids-safety-reporting-requirements-to-health-canada-2020-2021.pdf

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Health Canada Publishes Guidance for Industry on the Reporting …

(8 days ago) WEBOn July 8, 2015, Health Canada released important guidance designed to help consumer product companies, including retailers, understand their incident reporting obligations …

https://www.stikeman.com/en-ca/kh/canadian-product-liability-law/health-canada-publishes-guidance-for-industry-on-the-reporting-of-incidents-involving-consumer-products

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Medical Devices Regulations ( SOR /98-282) - Site Web de la

(9 days ago) WEB68.27 - Incident Reporting; 68.3 - Serious Risk of Injury to Human Health; 68.31 - Summary Report; 68.34 - Obligation to Submit Certificate; 68.35 - Sale — Cancellation …

https://laws-lois.justice.gc.ca/eng/regulations/SOR-98-282/

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