Regulations.gov document
Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance…
Notice · FDA-2012-N-0560 · posted Jun 12, 2012
Key facts
| Document ID | FDA-2012-N-0560-0001 |
|---|---|
| Title | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens Not Individually Identifiable |
| Document type | Notice |
| Subtype | 60 Day Proposed Information Collection |
| Agency | FDA |
| Docket | FDA-2012-N-0560 |
| Posted | Jun 12, 2012 |
| Federal Register citation | 77 FR 34954 |
| FR document number | 2012-14228 |
| Comment period opens | Jun 12, 2012 |
| Comments due | Aug 14, 2012 |
| Effective date | Jun 12, 2012 |
At a glance
- 1–9 Pages
- No Open for comment
- 1–9 Public comments on this docket
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