Guidance for market authorization requirements for COVID-19 drugs: Labelling and post-market requirements

A product monograph is a factual, scientific document on a drug product. It does not contain promotional material. The monograph describes the properties, claims, indications and conditions of use for the drug. It also contains any other information that may be required for optimal, safe and effective use of the drug.

Publisher
Health Canada
Resources
2
Catalogue metadata updated
2022-07-28

Data overview

Formats
HTML
File languages
English, French

Official sources and licences

Resources

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