{"id":507622,"title":"Health Canada IMDRF table of contents for medical device applications guidance - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-02-15","captureTimestamp":"2026-02-15T04:46:03.903000+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","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/507622","browseUrl":"https://replay.healtharchive.ca/job-6/20260215044603/https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum.html#ha_snapshot=507622","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}