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withdrawn,object_id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-2018-N-2727-0011,FDA,FDA-2018-N-2727,"Institutional Review Board Waiver or Alteration of Informed Consent for
Minimal Risk Clinical Investigations; Extension of Comment Period",Proposed Rule,Extension of Comment Period,2018-12-20T05:00:00Z,2018,12,2018-12-20T05:00:00Z,2019-02-14T04:59:59Z,2019-02-15T02:02:47Z,2018-27519,0,0,09000064839b9103
FDA-2018-N-3952-0057,FDA,FDA-2018-N-3952,Eliminating Youth Electronic Cigarette and Other Tobacco Product Use: The Role for Drug Therapies; New Date for Public Hearing; Request for  Comments,Proposed Rule,Request for Comment,2018-12-18T05:00:00Z,2018,12,2018-12-18T05:00:00Z,2019-02-02T04:59:59Z,2019-02-09T02:03:39Z,2018-27352,0,0,09000064839a99b2
FDA-2013-N-0500-0140,FDA,FDA-2013-N-0500,"Withdrawal of Proposed Rule on Supplemental Applications Proposing
Labeling Changes for Approved Drugs and Biological Products",Proposed Rule,Withdrawal,2018-12-14T05:00:00Z,2018,12,2018-12-14T05:00:00Z,,2018-12-14T14:36:07Z,2018-27098,0,0,09000064839936bc
FDA-2018-C-4464-0001,FDA,FDA-2018-C-4464,"Impossible Foods, Inc.; Filing of Color Additive Petition",Proposed Rule,Petition,2018-12-13T05:00:00Z,2018,12,2018-12-13T05:00:00Z,,2019-07-01T18:26:28Z,2018-26949,0,0,090000648398ed83
FDA-2018-N-2732-0001,FDA,FDA-2018-N-2732,Definition of the Term ‘‘Biological Product’’,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-12-12T05:00:00Z,2018,12,2018-12-12T05:00:00Z,2019-02-26T04:59:59Z,2019-02-26T02:03:21Z,2018-26840,0,0,0900006483987cd9
FDA-2018-N-0236-0001,FDA,FDA-2018-N-0236,Medical Device De Novo Classification Process,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-12-07T05:00:00Z,2018,12,2018-12-07T05:00:00Z,2019-03-08T04:59:59Z,2019-03-09T02:01:03Z,2018-26378,0,0,090000648395870c
FDA-2018-N-2727-0001,FDA,FDA-2018-N-2727,Institutional Review Board Waiver or Alteration of Informed Consent for Minimal Risk Clinical Investigations,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-11-15T05:00:00Z,2018,11,2018-11-15T05:00:00Z,2019-01-15T04:59:59Z,2019-01-15T02:01:45Z,2018-24822,0,0,09000064838d9668
FDA-2018-F-3757-0001,FDA,FDA-2018-F-3757,Flexible Vinyl Alliance; Filing of Food Additive Petition,Proposed Rule,Petition,2018-11-14T05:00:00Z,2018,11,2018-11-14T05:00:00Z,2019-01-15T04:59:59Z,2019-01-15T02:01:48Z,2018-24657,0,0,09000064838d4d64
FDA-2018-N-3952-0001,FDA,FDA-2018-N-3952,Eliminating Youth Electronic Cigarette and Other Tobacco Product Use: The Role for Drug Therapies; Public Hearing; Request for Comments,Proposed Rule,Notice of Hearing,2018-11-05T05:00:00Z,2018,11,2018-11-05T05:00:00Z,,2019-01-10T02:03:18Z,2018-24126,0,0,09000064838988db
FDA-2018-D-3631-0147,FDA,FDA-2018-D-3631,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Draft Guidance for Industry; Public Meetings; Request for Comments",Proposed Rule,Request for Comment,2018-11-01T04:00:00Z,2018,11,2018-11-01T04:00:00Z,2019-04-23T03:59:59Z,2019-04-24T01:01:36Z,2018-23868,0,0,090000648387abb1
FDA-2018-F-3932-0001,FDA,FDA-2018-F-3932,Bonamar Corp.; Filing of Food Additive Petition,Proposed Rule,Petition,2018-11-01T04:00:00Z,2018,11,2018-11-01T04:00:00Z,,2018-11-01T14:51:33Z,2018-23946,0,0,090000648387ac15
FDA-2016-N-2491-0024,FDA,FDA-2016-N-2491,"Withdrawal of the Laser Products; Proposed Amendment to Performance
Standard and the Electronic Submission of Labeling for Certain Home-Use Medical Devices",Proposed Rule,Withdrawal,2018-11-01T04:00:00Z,2018,11,2018-11-01T04:00:00Z,,2018-11-01T14:37:41Z,2018-23916,0,0,090000648387ac10
FDA-2011-N-0070-0036,FDA,FDA-2011-N-0070,"Withdrawal of the Laser Products; Proposed Amendment to Performance
Standard and the Electronic Submission of Labeling for Certain Home-Use Medical Devices",Proposed Rule,Withdrawal,2018-11-01T04:00:00Z,2018,11,2018-11-01T04:00:00Z,,2018-11-01T14:57:50Z,2018-23916,0,0,090000648387bc4a
FDA-2014-F-1184-0003,FDA,FDA-2014-F-1184,Zinpro Corp.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-10-30T04:00:00Z,2018,10,2018-10-30T04:00:00Z,,2018-10-30T13:53:00Z,2018-23672,0,0,09000064838687c9
FDA-2015-F-2712-0002,FDA,FDA-2015-F-2712,Adisseo France S.A.S.; Filing of Food Additive Petition (Animal Use),Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-10-30T04:00:00Z,2018,10,2018-10-30T04:00:00Z,,2018-10-30T13:43:52Z,2018-23671,0,0,0900006483868425
FDA-2018-D-3631-0001,FDA,FDA-2018-D-3631,"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Draft Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2018-10-22T04:00:00Z,2018,10,2018-10-22T04:00:00Z,2019-04-23T03:59:59Z,2019-04-24T01:03:00Z,2018-23006,0,0,0900006483837cda
FDA-2018-D-3583-0001,FDA,FDA-2018-D-3583,"Guide To Minimize Food Safety Hazards of Fresh-Cut Produce: Draft
Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2018-10-22T04:00:00Z,2018,10,2018-10-22T04:00:00Z,2019-04-23T03:59:59Z,2019-04-24T01:04:57Z,2018-23005,0,0,0900006483837d0c
FDA-2018-F-3347-0001,FDA,FDA-2018-F-3347,"Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use)",Proposed Rule,Petition,2018-10-02T04:00:00Z,2018,10,2018-10-02T04:00:00Z,2018-11-02T03:59:59Z,2018-10-27T01:03:26Z,2018-21395,0,0,0900006483789fcf
FDA-2005-N-0033-0014,FDA,FDA-2005-N-0033,Use of Materials Derived From Cattle in Medical Products Intended for Use in Humans and Drugs Intended for Use in Ruminants; Reporting Information Regarding Falsification of Data,Proposed Rule,Withdrawal,2018-09-28T04:00:00Z,2018,9,2018-09-28T04:00:00Z,,2018-10-23T15:00:58Z,2018-21133,0,0,090000648377f0ce
FDA-2007-N-0465-0028,FDA,FDA-2007-N-0465,"Label Requirement for Food That Has Been Refused Admission Into the
United States",Proposed Rule,Withdrawal,2018-09-28T04:00:00Z,2018,9,2018-09-28T04:00:00Z,,2018-10-23T15:19:14Z,2018-21145,0,0,090000648377f5a2
FDA-2008-N-0115-0050,FDA,FDA-2008-N-0115,Use of Materials Derived From Cattle in Medical Products Intended for Use in Humans and Drugs Intended for Use in Ruminants; Reporting Information Regarding Falsification of Data,Proposed Rule,Withdrawal,2018-09-28T04:00:00Z,2018,9,2018-09-28T04:00:00Z,,2018-10-23T15:02:03Z,2018-21133,0,0,090000648378011d
FDA-2018-N-3074-0001,FDA,FDA-2018-N-3074,Ophthalmic Devices; Reclassification of Ultrasound Cyclodestructive Device,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-09-25T04:00:00Z,2018,9,2018-09-25T04:00:00Z,2018-11-27T04:59:59Z,2024-05-20T14:09:47Z,2018-20763,0,0,090000648376da40
FDA-2018-F-3230-0001,FDA,FDA-2018-F-3230,Oakshire Naturals LP; Filing of Food Additive Petition,Proposed Rule,Petition,2018-09-18T04:00:00Z,2018,9,2018-09-18T04:00:00Z,,2018-09-18T13:56:42Z,2018-20217,0,0,090000648370f6f9
FDA-2018-N-1622-0001,FDA,FDA-2018-N-1622,Public Information,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-09-13T04:00:00Z,2018,9,2018-09-13T04:00:00Z,2018-11-14T04:59:59Z,2018-11-15T02:05:24Z,2018-19864,0,0,09000064836e6056
FDA-2018-N-0628-0001,FDA,FDA-2018-N-0628,"Medical Device Submissions: Amending Premarket Regulations That
Require Multiple Copies and Specify Paper Copies To Be Allowed in
Electronic Format",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-09-13T04:00:00Z,2018,9,2018-09-13T04:00:00Z,2018-12-13T04:59:59Z,2018-12-12T02:03:47Z,2018-19865,0,0,09000064836e65a5
FDA-2017-N-6924-0001,FDA,FDA-2017-N-6924,"Repeal of Regulation Requiring an Approved New Drug Application for
Drugs Sterilized by Irradiation",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-09-12T04:00:00Z,2018,9,2018-09-12T04:00:00Z,2018-11-14T04:59:59Z,2018-11-08T02:00:28Z,2018-19845,0,0,09000064836df353
FDA-2012-D-1002-0017,FDA,FDA-2012-D-1002,Supplemental Questions and Answers Regarding Food Facility Registration; Draft Guidance for Industry; Availability,Proposed Rule,GDL Guidance,2018-08-20T04:00:00Z,2018,8,2018-08-20T04:00:00Z,2018-10-20T03:59:59Z,2018-10-20T01:02:34Z,2018-17852,0,0,09000064836374ca
FDA-2018-N-3066-0001,FDA,FDA-2018-N-3066,Medical Devices: Classification of Accessories Distinct from Other Devices; Proposed List of Accessories Suitable for Class I; Request for Comments,Proposed Rule,Request for Comment,2018-08-17T04:00:00Z,2018,8,2018-08-17T04:00:00Z,2018-10-17T03:59:59Z,2018-10-17T01:07:07Z,2018-17731,0,0,0900006483630814
FDA-2018-N-2610-0001,FDA,FDA-2018-N-2610,"Future Format of the National Drug Code; Public Hearing; Request for
Comments",Proposed Rule,Request for Comment,2018-08-07T04:00:00Z,2018,8,2018-08-07T04:00:00Z,2019-01-06T04:59:59Z,2019-01-31T02:07:01Z,2018-16807,0,0,09000064835e0f0a
FDA-2018-N-2689-0001,FDA,FDA-2018-N-2689,Facilitating Competition and Innovation in the Biological Products Marketplace; Public Hearing; Request for Comments,Proposed Rule,Notice of Hearing,2018-07-25T04:00:00Z,2018,7,2018-07-25T04:00:00Z,2018-09-22T03:59:59Z,2018-10-11T01:31:25Z,2018-15859,0,0,0900006483554ac4
FDA-2014-F-2307-0003,FDA,FDA-2014-F-2307,"Humic Product Trade Association; Withdrawal of Food Additive Petition
(Animal Use)",Proposed Rule,Withdrawal,2018-07-19T04:00:00Z,2018,7,2018-07-19T04:00:00Z,,2018-07-19T13:34:40Z,2018-15394,0,0,090000648351f9f4
FDA-1992-N-0455-0001,FDA,FDA-1992-N-0455,Food Additives; Threshold of Regulation for Substances Used in Food-Contact Articles,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-07-13T04:00:00Z,2018,7,1993-10-12T04:00:00Z,1993-12-14T04:59:59Z,2018-07-14T01:05:30Z,1993-24940,0,0,0900006480532844
FDA-1992-N-0455-0019,FDA,FDA-1992-N-0455,Food Additives; Threshold of Regulation for Substances Used In Food-Contact Articles; Extension of Comment Period,Proposed Rule,Notice of Extension,2018-07-13T04:00:00Z,2018,7,2018-07-13T04:00:00Z,1994-02-12T04:59:59Z,2018-07-14T01:07:27Z,1993-30426,0,0,090000648053284b
FDA-2011-F-0171-0291,FDA,FDA-2011-F-0171,"Food Labeling: Calorie Labeling of Articles of Food Sold From Certain
Vending Machines; Front of Package Type Size",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-07-12T04:00:00Z,2018,7,2018-07-12T04:00:00Z,2018-09-26T03:59:59Z,2018-09-26T01:04:47Z,2018-14906,0,0,09000064834d7dd7
FDA-2018-N-2309-0001,FDA,FDA-2018-N-2309,The Food and Drug Administration Predictive Toxicology Roadmap and Its Implementation; Public Hearing; Request for Comments,Proposed Rule,Request for Comment,2018-06-29T04:00:00Z,2018,6,2018-06-29T04:00:00Z,2018-10-13T03:59:59Z,2018-10-14T01:02:31Z,2018-14052,0,0,0900006483478bc3
FDA-2017-N-6565-15120,FDA,FDA-2017-N-6565,Regulation of Flavors in Tobacco Products; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2018-06-08T04:00:00Z,2018,6,,,2018-06-08T17:07:42Z,2018-12369,0,0,0900006483398c5a
FDA-2017-N-6107-3431,FDA,FDA-2017-N-6107,Regulation of Premium Cigars; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2018-06-08T04:00:00Z,2018,6,2018-06-08T04:00:00Z,,2018-07-16T08:46:00Z,2018-12367,0,0,0900006483398bd2
FDA-2017-N-6189-0650,FDA,FDA-2017-N-6189,"Tobacco Product Standard for Nicotine Level of Combusted Cigarettes;
Extension of Comment Period",Proposed Rule,Extension of Comment Period,2018-06-08T04:00:00Z,2018,6,2018-06-08T04:00:00Z,,2018-07-16T08:46:05Z,2018-12368,0,0,09000064833985aa
FDA-2004-N-0191-0005,FDA,FDA-2004-N-0191,Product Jurisdiction: Correction,Proposed Rule,Correction,2018-06-07T04:00:00Z,2018,6,2018-06-07T04:00:00Z,2018-07-17T03:59:59Z,2025-04-11T18:29:27Z,2018-12201,0,0,090000648336367b
FDA-2018-N-1553-0001,FDA,FDA-2018-N-1553,Radiology Devices; Reclassification of Medical Image Analyzers,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-06-04T04:00:00Z,2018,6,2018-06-04T04:00:00Z,2018-08-04T03:59:59Z,2018-08-03T01:11:21Z,2018-11880,0,0,090000648332f8fa
FDA-2015-F-3663-0014,FDA,FDA-2015-F-3663,Grocery Manufacturers Association; Denial of Food Additive Petition,Proposed Rule,Denial,2018-05-21T04:00:00Z,2018,5,2018-05-21T04:00:00Z,2018-06-21T03:59:59Z,2018-06-19T01:03:40Z,2018-10715,0,0,09000064832a0740
FDA-2004-N-0191-0004,FDA,FDA-2004-N-0191,Product Jurisdiction,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-05-15T04:00:00Z,2018,5,2018-05-15T04:00:00Z,2018-07-17T03:59:59Z,2025-04-11T18:28:38Z,2018-10321,0,0,09000064832686f5
FDA-1977-N-0025-0231,FDA,FDA-1977-N-0025,"Tentative Final Monographs: Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Use; Partial Withdrawal",Proposed Rule,Withdrawal,2018-05-14T04:00:00Z,2018,5,2018-05-14T04:00:00Z,,2018-05-14T20:35:15Z,2018-10194,0,0,0900006483262e32
FDA-2018-D-0075-0083,FDA,FDA-2018-D-0075,"The Declaration of Added Sugars on Honey, Maple Syrup, and Certain
Cranberry Products: Draft Guidance for Industry; Extension of Comment
Period",Proposed Rule,Extension of Comment Period,2018-04-25T04:00:00Z,2018,4,2018-04-25T04:00:00Z,2018-06-16T03:59:59Z,2018-05-11T01:05:40Z,2018-08603,0,0,09000064831c0e39
FDA-2018-C-1007-0002,FDA,FDA-2018-C-1007,Aker BioMarine; Filing of Color Additive Petition,Proposed Rule,Petition,2018-04-09T04:00:00Z,2018,4,2018-04-09T04:00:00Z,2018-05-10T03:59:59Z,2018-05-10T01:02:04Z,2018-07155,0,0,09000064830dd241
FDA-2018-N-1214-0001,FDA,FDA-2018-N-1214,Medical Gas Regulation; Public Workshop; Request for Comments,Proposed Rule,Request for Comment,2018-03-29T04:00:00Z,2018,3,2018-03-29T04:00:00Z,2018-08-10T03:59:59Z,2024-11-07T01:23:47Z,2018-06251,1,0,0900006483061a32
FDA-2017-N-6107-0001,FDA,FDA-2017-N-6107,Regulation of Premium Cigars,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2018-03-26T04:00:00Z,2018,3,2018-03-26T04:00:00Z,2018-06-26T03:59:59Z,2018-04-28T01:03:00Z,2018-06047,0,0,090000648304d9a4
FDA-2017-N-6565-0001,FDA,FDA-2017-N-6565,Regulation of Flavors in Tobacco Products,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2018-03-21T04:00:00Z,2018,3,2018-03-21T04:00:00Z,2018-07-20T03:59:59Z,2024-05-30T01:03:28Z,2018-05655,0,0,09000064830358de
FDA-2008-N-0424-0022,FDA,FDA-2008-N-0424,Postmarketing Safety Reporting for Combination Products; Draft Guidance for Industry and Food and Drug Administration Staff; Availability,Proposed Rule,GDL Guidance,2018-03-21T04:00:00Z,2018,3,2018-03-21T04:00:00Z,2018-06-20T03:59:59Z,2018-03-21T13:13:54Z,2018-05687,0,0,09000064830356f0
FDA-2018-D-0671-0001,FDA,FDA-2018-D-0671,Determining the Number of Employees for Purposes of the ‘‘Small Business’’ Definition in Parts 117 and 507: Draft Guidance for Industry; Availability,Proposed Rule,GDL Guidance,2018-03-20T04:00:00Z,2018,3,2018-03-20T04:00:00Z,2018-05-22T03:59:59Z,2018-03-22T13:00:37Z,2018-05705,0,0,090000648302a4c1
FDA-2017-N-6189-0001,FDA,FDA-2017-N-6189,Tobacco Product Standard for Nicotine Level of Combusted Cigarettes,Proposed Rule,Advance Notice of Proposed Rulemaking (ANPRM),2018-03-16T04:00:00Z,2018,3,2018-03-16T04:00:00Z,2018-06-15T03:59:59Z,2018-04-29T01:01:18Z,2018-05345,0,0,090000648301bf2e
FDA-2014-F-0469-0002,FDA,FDA-2014-F-0469,Excentials B.V.; Withdrawal of Food Additive Petition (Animal Use),Proposed Rule,Withdrawal,2018-03-12T04:00:00Z,2018,3,2018-03-12T04:00:00Z,,2018-03-13T14:23:45Z,2018-04775,0,0,0900006482ffda8c
FDA-2018-C-0617-0002,FDA,FDA-2018-C-0617,GW Cosmetics GmbH; Filing of Color Additive Petition,Proposed Rule,Petition,2018-03-07T05:00:00Z,2018,3,2018-03-07T05:00:00Z,2018-04-07T03:59:59Z,2018-04-06T01:04:20Z,2018-04619,0,0,0900006482fa1256
FDA-2018-D-0075-0001,FDA,FDA-2018-D-0075,"The Declaration of Added Sugars on Honey, Maple Syrup, and Certain
Cranberry Products; Draft Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2018-03-02T05:00:00Z,2018,3,2018-03-02T05:00:00Z,2018-05-02T03:59:59Z,2018-04-29T01:01:05Z,2018-04281,0,0,0900006482f8584a
FDA-2018-N-0128-0001,FDA,FDA-2018-N-0128,"Nicotine Steering Committee; Establishment of a Public Docket;
Request for Comments",Proposed Rule,Request for Comment,2018-02-20T05:00:00Z,2018,2,2018-02-20T05:00:00Z,2018-04-17T03:59:59Z,2018-04-17T01:01:26Z,2018-03341,0,0,0900006482f453db
FDA-2017-N-6381-0001,FDA,FDA-2017-N-6381,Postmarketing Safety Reports for Approved New Animal Drugs; Electronic Submission Requirements,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-02-14T05:00:00Z,2018,2,2018-02-14T05:00:00Z,2018-05-01T03:59:59Z,2018-04-26T01:05:34Z,2018-02757,0,0,0900006482f30507
FDA-2017-N-7007-0002,FDA,FDA-2017-N-7007,Removal of Certain Time of Inspection and Duties of Inspector Regulations for Biological Products; Companion to Direct Final Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-01-26T05:00:00Z,2018,1,2018-01-26T05:00:00Z,2018-04-12T03:59:59Z,2018-04-13T01:01:40Z,2018-01467,0,0,0900006482e6bea2
FDA-2017-D-0397-0003,FDA,FDA-2017-D-0397,"Considerations for Determining Whether a Measure Provides the Same
Level of Public Health Protection as the Corresponding Requirement in 21 CFR Part 112 or the Preventive Controls Requirements in Part 117 or
507; Draft Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2018-01-25T05:00:00Z,2018,1,2018-01-25T05:00:00Z,2018-05-26T03:59:59Z,2018-01-25T23:07:09Z,2018-01296,0,0,0900006482e64592
FDA-2011-N-0143-0400,FDA,FDA-2011-N-0143,"Foreign Supplier Verification Programs for Importers of Food for Humans and Animals: What You Need To Know About the Food and Drug
Administration Regulation; Small Entity Compliance Guide; Availability",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-01-25T05:00:00Z,2018,1,2018-01-25T05:00:00Z,,2018-01-26T17:52:44Z,2018-01300,0,0,0900006482e6458d
FDA-2017-D-5225-0003,FDA,FDA-2017-D-5225,Foreign Supplier Verification Programs for Importers of Food for Humans and Animals; Draft Guidance for Industry; Availability,Proposed Rule,GDL Guidance,2018-01-25T05:00:00Z,2018,1,2018-01-25T05:00:00Z,2018-05-26T03:59:59Z,2023-01-11T19:13:39Z,2018-01297,0,0,0900006482e645c5
FDA-2017-D-6592-0002,FDA,FDA-2017-D-6592,"Application of the Foreign Supplier Verification Program Regulation to
Importers of Grain Raw Agricultural Commodities: Guidance for Industry;
Availability",Proposed Rule,GDL Guidance,2018-01-25T05:00:00Z,2018,1,2018-01-25T05:00:00Z,,2018-01-25T23:19:32Z,2018-01298,0,0,0900006482e645c4
FDA-2016-D-2343-0042,FDA,FDA-2016-D-2343,"Hazard Analysis and Risk-Based Preventive Controls for Human Food;
Draft Guidance for Industry; Availability",Proposed Rule,GDL Guidance,2018-01-25T05:00:00Z,2018,1,2018-01-25T05:00:00Z,2018-05-26T03:59:59Z,2024-05-31T13:17:23Z,2018-01299,0,0,0900006482e6461c
FDA-2017-N-5319-0007,FDA,FDA-2017-N-5319,"Devices Proposed for a New Use With an Approved, Marketed Drug; Public Hearing; Reopening of the Comment Period",Proposed Rule,Extension of Comment Period,2018-01-22T05:00:00Z,2018,1,2018-01-22T05:00:00Z,2018-02-22T04:59:59Z,2018-02-24T02:01:42Z,2018-00991,0,0,0900006482e3eea7
FDA-2016-D-3548-0001,FDA,FDA-2016-D-3548,"Public Warning and Notification of Recalls Under 21 CFR Part 7, Subpart
C; Draft Guidance for Industry and Food and Drug Administration Staff;
Availability",Proposed Rule,GDL Guidance,2018-01-19T05:00:00Z,2018,1,2018-01-19T05:00:00Z,2018-03-21T03:59:59Z,2018-03-21T13:03:35Z,2018-00918,0,0,0900006482e2ebf3
FDA-2016-N-2378-0001,FDA,FDA-2016-N-2378,Internal Agency Review of Decisions; Requests for Supervisory Review of Certain Decisions Made by Center for Devices and Radiological Health,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-01-17T05:00:00Z,2018,1,2018-01-17T05:00:00Z,2018-04-18T03:59:59Z,2018-04-18T01:04:11Z,2018-00646,0,0,0900006482e18ba5
FDA-2017-N-0763-0867,FDA,FDA-2017-N-0763,Food Labeling: Health Claims; Soy Protein and Coronary Heart Disease; Extension of Comment Period,Proposed Rule,Extension of Comment Period,2018-01-17T05:00:00Z,2018,1,2018-01-17T05:00:00Z,2018-03-20T03:59:59Z,2023-08-08T01:02:42Z,2018-00683,0,0,0900006482e18b55
FDA-2015-N-2002-2008,FDA,FDA-2015-N-2002,"Clarification of When Products Made or Derived From Tobacco Are
Regulated as Drugs, Devices, or Combination Products; Amendments
to Regulations Regarding ‘‘Intended Uses’’; Proposed Partial Delay of
Effective Date",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2018-01-16T05:00:00Z,2018,1,2018-01-16T05:00:00Z,2018-02-06T04:59:59Z,2018-02-06T14:02:16Z,2018-00555,0,0,0900006482e0b3c7