documents: HHS-OPHS-2015-0002-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HHS-OPHS-2015-0002-0001 | HHS | HHS-OPHS-2015-0002 | Draft Guidance for Industry, Clinical Investigators, and Institutional Review Boards—Use of an Electronic Informed Consent in Clinical Investigations - Questions and Answers; Availability | Notice | 2015-03-09T04:00:00Z | 2015 | 3 | 2015-03-09T04:00:00Z | 2015-05-08T03:59:59Z | 2015-05-18T13:24:58Z | 2015-05301 | 0 | 0 | 0900006481a3403f |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref