documents: FDA-2017-D-1105-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2017-D-1105-0001 | FDA | FDA-2017-D-1105 | Use of Electronic Records and Electronic Signatures in Clinical Investigations Under Part 11— Questions and Answers; Draft Guidance for Industry; Availability | Proposed Rule | Request for Comment | 2017-06-21T04:00:00Z | 2017 | 6 | 2017-06-21T04:00:00Z | 2017-08-22T03:59:59Z | 2017-08-22T13:48:40Z | 2017-12811 | 0 | 0 | 0900006482711aad |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref