dockets: FDA-2018-N-2727

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

This data as json

id	agency_id	title	docket_type	last_modified	object_id	rin	dkabstract	category	subtype	keywords	program	short_title	effective_date	organization	attrs_raw	attr_source
FDA-2018-N-2727	FDA	Institutional Review Board Waiver or Alteration of Informed Consent for Minimal Risk Clinical Investigations	Nonrulemaking	2024-01-18T08:44:49Z	0b000064834ed7f4					["CDER"]	CDER				{"displayProperties": [{"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}], "keywords": ["CDER"], "modifyDate": "2024-01-18T08:44:49Z", "dkAbstract": null, "agencyId": "FDA", "program": "CDER", "shortTitle": null, "subType2": null, "title": "Institutional Review Board Waiver or Alteration of Informed Consent for Minimal Risk Clinical Investigations", "generic": "N", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": null, "subType": null, "category": null, "field2": null, "effectiveDate": null, "objectId": "0b000064834ed7f4"}	single_get

Links from other tables