Guidance for market authorization requirements for COVID-19 drugs: Rolling submissions and reviews (French, HTML)
View metadata and access the original French HTML file: Guidance for market authorization requirements for COVID-19 drugs: Rolling submissions and reviews.
- Format
- HTML
- Access
- file-only
- Publisher-reported update
- 2022-07-28
Modified requirements for COVID-19 drugs allow for the filing of rolling submissions (section C.08.002(2.3) of Canada's Food and Drug Regulations). The ability to review data from early development while later-stage clinical trials are taking place helps to expedite the regulatory review process.
Data overview
- Formats
- HTML
- File languages
- French
- Available actions
- Access original file