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

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

This is a public health concern resulting in significant costs to the health care system as well as individual impacts on Canadians. Health Canada's monitoring of therapeutic product safety plays a vital role in public health and patient safety, providing health care providers and patients with the most up-to-date knowledge for decision making. It also provides Health Canada with information needed to monitor the benefit-risk ratio of products and act to protect Canadians where appropriate.

Publisher: Health Canada
Resources: 2
Catalogue metadata updated: 2022-10-21

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

Related open data

Health Canada