Guidance for market authorization requirements for COVID-19 drugs: Labelling and post-market requirements (English, HTML)

View metadata and access the original English HTML file: Guidance for market authorization requirements for COVID-19 drugs: Labelling and post-market requirements.

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Publisher-reported update

2022-07-28

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.

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