Regulations.gov document
Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance…
Notice · FDA-2014-D-2138 · posted Jun 21, 2018
Key facts
| Document ID | FDA-2014-D-2138-0017 |
|---|---|
| Title | Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry: Adverse Event Reporting for Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act |
| Document type | Notice |
| Subtype | 60 Day Proposed Information Collection |
| Agency | FDA |
| Docket | FDA-2014-D-2138 |
| Posted | Jun 21, 2018 |
| Federal Register citation | 83 FR 28854 |
| FR document number | 2018-13294 |
| Comment period opens | Jun 21, 2018 |
| Comments due | Aug 21, 2018 |
| Effective date | Jun 21, 2018 |
At a glance
- 1–9 Pages
- No Open for comment
- 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: