SUBPART B—Generally Applicable Requirements for Individual Adverse Event Reports (§803.20 to §803.22) - Title 21 - Food and Drugs CFR - USA Laws Searching

CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898) > PART 803—MEDICAL DEVICE REPORTING > SUBPART B—Generally Applicable Requirements for Individual Adverse Event Reports (§803.20 to §803.22)

SUBPART B—Generally Applicable Requirements for Individual Adverse Event Reports (§803.20 to §803.22)

803.20—How do I complete and submit an individual adverse event report?
803.21—Where can I find the reporting codes for adverse events that I use with medical device reports?
803.22—What are the circumstances in which I am not required to file a report?