documents: FDA-2015-D-0390-0025
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | agency_id | docket_id | title | document_type | subtype | posted_date | posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2015-D-0390-0025 | FDA | FDA-2015-D-0390 | Use of Electronic Informed Consent—Questions and Answers; Guidance for Institutional Review Boards, Investigators, and Sponsors; Availability | Notice | Notice of Availability | 2016-12-15T05:00:00Z | 2016 | 12 | 2016-12-15T05:00:00Z | 2016-12-15T15:09:26Z | 2016-30146 | 0 | 0 | 090000648240b6b5 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref