21 CFR Part 803 - MEDICAL DEVICE REPORTING
- Subpart A - General Provisions (§§ 803.1 - 803.19)
- Subpart B - Generally Applicable Requirements for Individual Adverse Event Reports (§§ 803.20 - 803.23)
- Subpart C - User Facility Reporting Requirements (§§ 803.30 - 803.33)
- Subpart D - Importer Reporting Requirements (§§ 803.40 - 803.42)
- Subpart E - Manufacturer Reporting Requirements (§§ 803.50 - 803.58)
The following state regulations pages link to this page.
Virginia