Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Overview

Name: Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Overview
Creator: Health Canada
License: https://open.canada.ca/en/open-government-licence-canada

The purpose of this guidance document is to provide hospitals with information that may be useful in achieving compliance with the federal regulatory requirement for hospitals to report serious ADRs and MDIs to Health Canada as outlined in section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Device Regulations.

Publisher: Health Canada
Resources: 2
Catalogue metadata updated: 2021-06-01

Data overview

Formats: HTML
File languages: English, French

Official sources and licences

Government of Canada Open Data
Open Government Licence – Canada

Resources

Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Overview (French, HTML) HTML
Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Overview (English, HTML) HTML

Related open data

Health Canada