{"data":{"id":"us/21-cfr-803.23","jurisdiction":"us","citation":"21 CFR 803.23","heading":"Where can I find information on how to prepare and submit an MDR in electronic format?","body":"(a) You may obtain information on how to prepare and submit reports in an electronic format that FDA can process, review, and archive at: http://www.fda.gov/ForIndustry/FDAeSubmitter/ucm107903.htm.\n(b) We may sometimes update information on how to prepare and submit reports electronically. If we do make modifications, we will ensure that we alert reporters by updating the eMDR Web page.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 803—MEDICAL DEVICE REPORTING","Subpart B—Generally Applicable Requirements for Individual Adverse Event Reports"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"dd9d19d140bde99f2e3d28edf8556e859585a7ca402e20457884c3774a68c80b","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-803.22","next":"us/21-cfr-803.30"},"notice":"GroundRules: Original legal text. Not legal advice."}