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Draft Health Canada IMD RF table of contents for medical device applications guidance On this page 1. Introduction and background o 1.1 Purpose o 1.2 Scope and application 1.2.1 Structure guidance
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The draft Health Canada IMDRF is a form used by medical device manufacturers to submit information about their products to Health Canada.
Medical device manufacturers are required to file the draft Health Canada IMDRF.
The draft Health Canada IMDRF can be filled out online through Health Canada's portal with the required information about the medical device.
The purpose of the draft Health Canada IMDRF is to ensure that medical devices meet regulatory standards for safety and effectiveness.
Information such as device classification, intended use, design specifications, clinical data, and risk assessment must be reported on the draft Health Canada IMDRF.
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