Regulations.gov document
Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission…
Rule · FDA-2008-N-0334 · posted Jun 10, 2014
Key facts
| Document ID | FDA-2008-N-0334-0009 |
|---|---|
| Title | Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission Requirements |
| Document type | Rule |
| Subtype | Final Rule |
| Agency | FDA |
| Docket | FDA-2008-N-0334 |
| Posted | Jun 10, 2014 |
| Federal Register citation | 79 FR 33072 |
| FR document number | 2014-13480 |
| CFR | 21 CFR Parts 310, 314, 329, and 600 |
| Comment period opens | Jun 10, 2014 |
| Effective date | Jun 10, 2014 |
At a glance
- 10–99 Pages
- 1–9 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: