Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Guidance document (English, HTML)
View metadata and access the original English HTML file: Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Guidance document.
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- Publisher-reported update
- 2022-10-21
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.
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