Regulations.gov document
Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act…
Notice · FDA-2011-D-0514 · posted Oct 7, 2022
Key facts
| Document ID | FDA-2011-D-0514-0026 |
|---|---|
| Title | Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act; Guidance for Industry and Food and Drug Administration Staff; and Procedures for Handling Post-Approval Studies Imposed by Premarket Approval Application Order; Guidance for Industry and Food and Drug Administration Staff; Availability - Final Guidance |
| Document type | Notice |
| Subtype | Notice of Availability |
| Agency | FDA |
| Docket | FDA-2011-D-0514 |
| Posted | Oct 7, 2022 |
| Federal Register citation | 87 FR 61030 |
| FR document number | 2022-21832 |
| Comment period opens | Oct 7, 2022 |
| Effective date | Oct 7, 2022 |
At a glance
- 1–9 Pages
- 10–99 Public comments on this docket
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Regulations.gov documents
Regulations.gov holds the rulemaking and other documents federal agencies post for public comment. Only agency documents are published here; public submissions are not.
Source: Regulations.gov (U.S. General Services Administration eRulemaking Program) · Source date: