{"id":434146,"title":"Health Canada IMDRF table of contents for medical device applications guidance - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-01-02","captureTimestamp":"2026-01-02T11:31:22.789000+00:00","jobId":6,"originalUrl":"https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum.html?wbdisable=true","snippet":"Health Canada IMDRF table of contents for medical device applications guidance Download in PDF format (551 KB, 13 pages) Organization: Health Canada Date published: 2025-11-25 On this page Introduction and background Guidance for implementation Filing process Resources, tools and…","rawSnapshotUrl":"/api/snapshots/raw/434146","browseUrl":"https://replay.healtharchive.ca/job-6/20260102113122/https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum.html?wbdisable=true#ha_snapshot=434146","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}