Regulations.gov document
Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance…
Notice · FDA-2011-N-0915 · posted Jan 23, 2015
Key facts
| Document ID | FDA-2011-N-0915-0003 |
|---|---|
| Title | Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application |
| Document type | Notice |
| Subtype | 60 Day Proposed Information Collection |
| Agency | FDA |
| Docket | FDA-2011-N-0915 |
| Posted | Jan 23, 2015 |
| Federal Register citation | FR 80 3608 |
| FR document number | 2015-01111 |
| Comment period opens | Jan 23, 2015 |
| Comments due | Mar 25, 2015 |
| Effective date | Jan 23, 2015 |
At a glance
- 1–9 Pages
- No Open for comment
- 1–9 Public comments on this docket
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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