{"id":372410,"title":"Lot Release - Guidance Documents - Applications and Submissions - Biologics, Radiopharmaceuticals and Genetic Therapies - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-04-11","captureTimestamp":"2026-04-11T16:51:29.440000+00:00","jobId":6,"originalUrl":"https://www.canada.ca/en/health-canada/services/drugs-health-products/biologics-radiopharmaceuticals-genetic-therapies/applications-submissions/guidance-documents/release.html","snippet":"Lot Release - Guidance Documents - Applications and Submissions - Biologics, Radiopharmaceuticals and Genetic Therapies Section C.04.015 of the Food and Drugs Act and Regulations , states that \"on written request from the Director, every fabricator, packager/labeller, tester,…","rawSnapshotUrl":"/api/snapshots/raw/372410","browseUrl":"https://replay.healtharchive.ca/job-6/20260411165129/https://www.canada.ca/en/health-canada/services/drugs-health-products/biologics-radiopharmaceuticals-genetic-therapies/applications-submissions/guidance-documents/release.html#ha_snapshot=372410","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}