Regulations.gov document
Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance…
Notice · FDA-2012-N-0560 · posted Oct 23, 2015
Key facts
| Document ID | FDA-2012-N-0560-0004 |
|---|---|
| Title | Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens That Are Not Individually Identifiable |
| Document type | Notice |
| Subtype | 60 Day Proposed Information Collection |
| Agency | FDA |
| Docket | FDA-2012-N-0560 |
| Posted | Oct 23, 2015 |
| Federal Register citation | 80 FR 64422 |
| FR document number | 2015-26985 |
| Comment period opens | Oct 23, 2015 |
| Comments due | Dec 23, 2015 |
| Effective date | Oct 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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