Applications for medical devices under the Interim Order for use in relation to COVID-19 - Guidance document (English, HTML)

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Publisher-reported update

2020-04-07

Guidance documents are administrative instruments not having force of law and, as such, allow for flexibility in approach. This guidance document is intended to provide guidance to manufacturers and importers to organize and submit an application in a timely manner for the sale or importation of medical devices that are manufactured, sold or represented for use in relation to COVID-19.

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