Regulations.gov document
Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance…
Notice · FDA-2011-N-0915 · posted Dec 27, 2011
Key facts
| Document ID | FDA-2011-N-0915-0001 |
|---|---|
| Title | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products, etc. |
| Document type | Notice |
| Subtype | General Notice |
| Agency | FDA |
| Docket | FDA-2011-N-0915 |
| Posted | Dec 27, 2011 |
| Federal Register citation | 76 FR 80946 |
| FR document number | 2011-33140 |
| Comment period opens | Dec 27, 2011 |
| Comments due | Feb 28, 2012 |
| Effective date | Dec 27, 2011 |
At a glance
- 1–9 Pages
- No Open for comment
- 1–9 Public comments on this docket
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