documents

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

526 rows where agency_id = "FDA", document_type = "Notice" and posted_year = 2006 sorted by posted_date descending

✎ View and edit SQL

This data as json, CSV (advanced)

Suggested facets: posted_month, open_for_comment, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)

posted_year 1

  • 2006 · 526 ✖

document_type 1

  • Notice · 526 ✖

agency_id 1

  • FDA · 526 ✖
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2003-N-0385-0001 FDA Draft Animal Cloning Risk Assessment re FDA-2008-N-0033 FDA-2003-N-0385 FDA Notice NAD-Notice of Availability of Data 2006-12-28T05:00:00Z 2006 12 2006-12-28T05:00:00Z 2007-04-03T03:59:59Z 2008-04-12T01:03:44Z   0 0 090000648049a462
FDA-2006-P-0074-0007 FDA To Exempt the Class II device Cranial Orthoses from Premarket Notification Requirements under section 510(m)(2)-CLOSED FDA-2006-P-0074 FDA Notice N-Notice 2006-12-26T05:00:00Z 2006 12 2006-12-22T05:00:00Z   2008-04-11T23:17:41Z   0 0 0900006480444652
FDA-2006-D-0032-0005 FDA Guidance for Clinical Investigators, Institutional Review Boards and Sponsors Process for Handling Referrals to FDA Under 21 CFR 50.54 : Additional Safeguards for Children in Clinical Investigations FDA-2006-D-0032 FDA Notice NAD-Notice of Availability of Data 2006-12-22T05:00:00Z 2006 12 2006-12-21T05:00:00Z   2008-04-11T22:52:06Z   0 0 09000064804420d6
FDA-2006-N-0042-0002 FDA Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment FDA-2006-N-0042 Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment (DUPLICATE) Notice Notice of Final Rule 2006-12-22T05:00:00Z 2006 12 2006-12-22T05:00:00Z   2025-07-09T00:26:29Z E6-21952 0 0 09000064804428d5
FDA-2006-N-0042-0001 FDA Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment FDA-2006-N-0042 Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment Notice Notice of Final Rule 2006-12-22T05:00:00Z 2006 12 2006-12-22T05:00:00Z   2025-07-09T00:24:56Z E6-21952 0 0 09000064804428d6
FDA-2005-D-0027-0004 FDA Guidance for Industry and Food and Drug Administration: Procedures for Handling Post-Approval Studies Imposed by PMA Order FDA-2005-D-0027 FDA Notice NAD-Notice of Availability of Data 2006-12-21T05:00:00Z 2006 12 2006-12-20T05:00:00Z   2008-04-11T23:46:25Z   0 0 090000648043e843
FDA-2003-D-0030-0012 FDA Guidance on Marketed Unapproved Drugs Compliance Policy Guide FDA-2003-D-0030 FDA Notice N-Notice 2006-12-20T05:00:00Z 2006 12     2008-04-12T00:54:03Z   0 0 090000648048154e
FDA-2006-N-0420-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Product Jurisdiction: Assignment of Agency Component for Review of Premarket Applications FDA-2006-N-0420 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Product Jurisdiction: Assignment of Agency Component for Review of Premarket Applications Notice General Notice 2006-12-20T05:00:00Z 2006 12 2006-12-20T05:00:00Z 2007-01-20T04:59:59Z 2025-06-18T22:33:57Z E6-21636 0 0 09000064804617a1
FDA-2006-N-0046-0005 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Prior Notice of Imported Food Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002 FDA-2006-N-0046 FDA Notice N-Notice 2006-12-20T05:00:00Z 2006 12 2006-12-19T05:00:00Z   2008-04-11T23:09:21Z   0 0 0900006480443f99
FDA-2003-N-0049-0025 FDA Patient Examination & Surgeons' Gloves; Test Procedures FDA-2003-N-0049 FDA Notice NFR-Notice of Final Rule 2006-12-19T05:00:00Z 2006 12 2006-12-18T05:00:00Z   2008-04-12T00:58:18Z   0 0 0900006480481999
FDA-2006-D-0158-0009 FDA Manufactured Food Regulatory Program Standards FDA-2006-D-0158 FDA Notice N-Notice 2006-12-18T05:00:00Z 2006 12 2006-12-15T05:00:00Z   2008-04-11T23:03:17Z   0 0 0900006480450675
FDA-2006-N-0498-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Experimental Study of Possible Footnotes and Cueing Schemes to Help Consumers Interpret Quantitative Trans Fat Disclosure on the Nutrition Facts Panel FDA-2006-N-0498 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Experimental Study of Possible Footnotes and Cueing Schemes to Help Consumers Interpret Quantitative Trans Fat Disclosure on the Nutrition Facts Panel Notice General Notice 2006-12-17T05:00:00Z 2006 12 2006-12-18T05:00:00Z 2006-12-19T04:59:59Z 2025-05-19T21:37:55Z E6-21486 0 0 0900006480463888
FDA-2006-N-0370-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Registration of Food Facilities Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002 FDA-2006-N-0370 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Registration of Food Facilities Under the Public Health Security and Bloterrorism Preparedness and Response Act of 2002 Notice General Notice 2006-12-15T05:00:00Z 2006 12 2006-12-15T05:00:00Z 2007-01-17T04:59:59Z 2025-06-17T21:38:04Z E6-21375 0 0 090000648045fe30
FDA-2006-N-0483-0001 FDA International Drug Scheduling; Convention on Psychotropic Substances; Single Convention on Narcotic Drugs; World Health Organization Scheduling Recommendations for Dronabinol (INN) and its Stereoisomers, and Oripavine FDA-2006-N-0483 International Drug Scheduling; Convention on Psychotropic Substances; Single Convention on Narcotic Drugs; World Health Organization Scheduling Recommendations for Dronabinol and its Stereolsomers, and Oripavine Notice General Notice 2006-12-15T05:00:00Z 2006 12 2006-12-14T05:00:00Z 2007-01-17T04:59:59Z 2025-07-09T00:08:54Z E6-21318 0 0 0900006480463157
FDA-2006-N-0234-0001 FDA Drug Products Containing Quinine; Enforcement Action Dates FDA-2006-N-0234 Drug Products Containing Quinine; Enforcement Action Dates Notice General Notice 2006-12-15T05:00:00Z 2006 12 2006-12-15T05:00:00Z   2025-07-09T00:02:25Z 06-9713 0 0 09000064804568dc
FDA-2006-N-0253-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Experimental Study of Trans Fat Claims on Foods FDA-2006-N-0253 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Proposed Experimental Study of Trans Fat Claims on Foods Notice General Notice 2006-12-14T05:00:00Z 2006 12 2006-12-15T05:00:00Z 2006-12-15T04:59:59Z 2025-05-20T15:12:37Z E6-21317 0 0 090000648045765f
FDA-2006-N-0419-0002 FDA Agency Information Collection Activities: Proposed Collection; Comment Request; Postmarket Surveillance FDA-2006-N-0419 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Postmarket Surveillance Notice General Notice 2006-12-13T05:00:00Z 2006 12 2006-12-13T05:00:00Z 2007-01-13T04:59:59Z 2025-07-01T19:21:35Z E6-21167 0 0 090000648046174a
FDA-1998-P-0086-0009 FDA Permit the label statement of "Supplement Facts" FDA-1998-P-0086 Notice of Final Rule re Permit the label statement of "Supplement Facts" Notice Notice of Final Rule 2006-12-13T05:00:00Z 2006 12 2006-12-12T05:00:00Z   2015-12-07T13:50:33Z   0 0 090000648058516b
FDA-2006-N-0246-0002 FDA Agency Information Collection Activities: Proposed Collection; Comment Request; Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format FDA-2006-N-0246 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format Notice General Notice 2006-12-12T05:00:00Z 2006 12 2006-12-13T05:00:00Z 2007-01-13T04:59:59Z 2025-05-22T16:22:18Z E6-21132 0 0 09000064804572fc
FDA-2006-N-0306-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602) FDA-2006-N-0306 Withdrawal of Federal Register Notice Notice Withdrawal 2006-12-07T05:00:00Z 2006 12 2006-12-07T05:00:00Z   2025-07-02T23:41:28Z E6-20705 0 0 090000648045c593
FDA-2005-N-0294-0008 FDA Color Additive Certification; Increase in Fees for Certification Services FDA-2005-N-0294 Color Additive Certification; Increase in Fees for Certification Services Notice Extension of Comment Period 2006-12-07T05:00:00Z 2006 12 2006-12-07T05:00:00Z 2007-02-06T04:59:59Z 2025-06-16T22:36:41Z   0 0 0900006480446aa5
FDA-2006-N-0183-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Establishing and Maintaining a List of U.S. Dairy Product Manufacturers/Processors With Interest in Exporting to Chile FDA-2006-N-0183 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Establishing and Maintaining a List of United States Dairy Product Manufacturers/ Processors With Interest in Exporting to Chile Notice General Notice 2006-12-07T05:00:00Z 2006 12 2006-12-07T05:00:00Z 2007-01-09T04:59:59Z 2025-06-19T00:02:22Z E6-20704 0 0 0900006480450db6
FDA-2006-N-0169-0001 FDA Use of Ozone-Depleting Substances; Removal of Essential Use Designations FDA-2006-N-0169 Use of Ozone-Depleting Substances; Removal of Essential Use Designations; Companion Document to Direct Final Rule Notice NPR-Notice of Proposed Rule-Making 2006-12-07T05:00:00Z 2006 12 2006-12-07T05:00:00Z 2007-02-21T04:59:59Z 2025-07-01T22:39:04Z E6-20796 0 0 0900006480450904
FDA-2006-N-0169-0002 FDA Use of Ozone-Depleting Substances; Removal of Essential Use Designations FDA-2006-N-0169 Use of Ozone-Depleting Substances; Removal of Essential Use Designations Notice Notice of Final Rule 2006-12-07T05:00:00Z 2006 12 2006-12-07T05:00:00Z 2007-02-21T04:59:59Z 2025-07-01T22:42:39Z E6-20797 0 0 0900006480450907
FDA-2006-N-0185-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Substances Prohibited from Use in Animal Food or Feed; Animal Proteins Prohibited in Ruminant Feed FDA-2006-N-0185 Agency Information Collection Activities; Proposed Collection; Comment Request; Substances Prohibited from Use in Animal Food or Feed; Animal Proteins Prohibited in Ruminant Feed Notice General Notice 2006-12-04T05:00:00Z 2006 12 2006-12-04T05:00:00Z 2007-02-03T04:59:59Z 2025-07-08T23:31:41Z E6-20476 0 0 0900006480450dd7
FDA-2006-N-0243-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Human Tissue Intended for Transplantation FDA-2006-N-0243 Agency Information Collection Activities; Proposed Collection; Comment Request; Human Tissue Intended for Transplantation Notice General Notice 2006-12-04T05:00:00Z 2006 12 2006-12-04T05:00:00Z 2007-02-03T04:59:59Z 2025-07-08T23:47:27Z E6-20477 0 0 0900006480457165
FDA-2005-N-0349-0002 FDA Cosmetic Labeling Regulations FDA-2005-N-0349 Agency In formation Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Cosmetic Labeling Regulations Notice 30 Day Proposed Information Collection 2006-12-04T05:00:00Z 2006 12 2006-12-01T05:00:00Z   2025-10-21T18:01:53Z E6-20478 0 0 0900006480449f95
FDA-2006-N-0109-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Food Labeling; Notification Procedures for Statements on Dietary Supplements FDA-2006-N-0109 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Food Labeling; Notification Procedures for Statements on Dietary Supplements Notice General Notice 2006-12-01T05:00:00Z 2006 12 2006-12-01T05:00:00Z 2007-01-03T04:59:59Z 2025-06-20T16:04:44Z E6-20307 0 0 0900006480450094
FDA-2006-D-0357-0004 FDA Guidance for Industry and Food and Drug Administration Staff; Commercially Distributed Analyte Specific Reagents (ASRs): Frequently Asked Questions FDA-2006-D-0357 FDA Notice NEC-Notice of Extension 2006-11-29T05:00:00Z 2006 11 2006-11-27T05:00:00Z 2007-03-06T04:59:59Z 2008-04-11T23:06:48Z   0 0 090000648045f784
FDA-2006-D-0233-0004 FDA Guidance for Industry, Clinical Laboratories, and FDA Staff on In Vitro Diagnostic Multivariate Index Assays FDA-2006-D-0233 FDA Notice NEC-Notice of Extension 2006-11-29T05:00:00Z 2006 11 2006-11-27T05:00:00Z 2007-03-06T04:59:59Z 2008-04-11T23:06:24Z   0 0 09000064804565b8
FDA-2005-N-0465-0005 FDA Agency Information Collection Activities: Proposed Collection; Comment Request; Experimental Study of Qualified Health Claims: Consumer Inferences about Omega-3 Fatty Acids and Monounsaturated Fatty Acids from Olive Oil FDA-2005-N-0465 Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Experimental Study of Qualified Health Claims: Consumer Inferences About Monounsaturated Fatty Acids From Olive Oil, EPA and Omega-3 Fatty Acids, and Green Tea Notice Notice of Approval 2006-11-29T05:00:00Z 2006 11 2006-11-28T05:00:00Z   2025-10-23T22:50:41Z E6-20200 0 0 0900006480450db4
FDA-2006-D-0233-0005 FDA Guidance for Industry, Clinical Laboratories, and FDA Staff on In Vitro Diagnostic Multivariate Index Assays FDA-2006-D-0233 FDA Notice NEC-Notice of Extension 2006-11-29T05:00:00Z 2006 11 2006-11-27T05:00:00Z 2007-03-06T04:59:59Z 2008-04-11T23:06:27Z   0 0 09000064804565b9
FDA-2006-N-0104-0001 FDA Improving Patient Safety by Enhancing the Container Labeling for Parenteral Infusion Drug Products; Public Meeting FDA-2006-N-0104 FDA Notice NM-Notice of Meeting 2006-11-29T05:00:00Z 2006 11 2006-11-27T05:00:00Z 2007-04-13T03:59:59Z 2008-04-11T23:09:30Z   0 0 090000648044f494
FDA-2005-D-0444-0004 FDA Guidance for Industry on Gene Therapy Clinical Trials Observing Participants for Delayed Adverse Events FDA-2005-D-0444 FDA Notice NAD-Notice of Availability of Data 2006-11-29T05:00:00Z 2006 11 2006-11-27T05:00:00Z   2008-04-11T23:47:35Z   0 0 09000064804505cc
FDA-2006-N-0247-0001 FDA Training Program for Regulatory Project Managers; Information Available to Industry FDA-2006-N-0247 Training Program for Regulatory Project Managers; Information Available to Industry Notice General Notice 2006-11-29T05:00:00Z 2006 11 2006-11-28T05:00:00Z 2007-01-30T04:59:59Z 2025-07-08T23:22:13Z E6-20041 0 0 090000648045730d
FDA-2005-D-0084-0016 FDA Guidance for Industry, Lead in Candy Likely To Be Consumed Frequently by Small Children: Recommended Maximum Level and Enforcement Policy, Availability; and draft supporting document, Supporting Document for Maximum Recommended Level for Lead in Candy Likely To Be Consumed Frequently By Small Children, FDA-2005-D-0084 FDA Notice NAD-Notice of Availability of Data 2006-11-24T05:00:00Z 2006 11 2006-11-22T05:00:00Z   2008-04-11T23:46:31Z   0 0 090000648043f477
FDA-2006-N-0106-0001 FDA Food Defense Workshop; Public Workshop FDA-2006-N-0106 Food Defense Workshop; Public Workshop Notice Meeting 2006-11-24T05:00:00Z 2006 11 2006-11-24T05:00:00Z   2025-07-08T20:51:03Z E6-19886 0 0 090000648044f5fd
FDA-2006-D-0475-0001 FDA Guidance for Industry, Food and Drug Administration Staff, Eye Care Professionals, and Consumers FDA-2006-D-0475 FDA Notice NAD-Notice of Availability of Data 2006-11-24T05:00:00Z 2006 11 2006-11-22T05:00:00Z   2008-04-11T23:07:12Z   0 0 0900006480462ec9
FDA-2006-D-0167-0001 FDA Guidance for Industry on Sinusitis: Designing Clinical Development Programs of Nonantimicrobial Drugs for Treatment; Availability FDA-2006-D-0167 FDA Notice NAD-Notice of Availability of Data 2006-11-21T05:00:00Z 2006 11 2006-11-21T05:00:00Z 2007-01-23T04:59:59Z 2008-04-11T23:03:22Z   0 0 0900006480450814
FDA-2004-D-0124-0004 FDA Guidance for Industry and FDA Staff; Saline, Silicone Gel, and Alternative Breast Implants FDA-2004-D-0124 FDA Notice NAD-Notice of Availability of Data 2006-11-21T05:00:00Z 2006 11 2006-11-17T05:00:00Z 2007-11-20T04:59:59Z 2008-04-12T00:34:43Z   0 0 090000648046fc8b
FDA-2006-N-0107-0001 FDA Electronic Submission of Regulatory Information, and Creating an Electronic Platform for Enhanced Information Management; Public Hearing FDA-2006-N-0107 FDA Notice NHC-Notice of Hearing Before Commissioner 2006-11-21T05:00:00Z 2006 11 2006-11-15T05:00:00Z 2006-12-09T04:59:59Z 2008-04-11T23:09:35Z   0 0 090000648044f679
FDA-2006-D-0160-0007 FDA Prescription Drug Marketing Act Pedigree Requirements under 21 CFR Part 203; Effective Date and Compliance Policy Guide FDA-2006-D-0160 FDA Notice NAD-Notice of Availability of Data 2006-11-15T05:00:00Z 2006 11 2006-11-14T05:00:00Z 2007-11-15T04:59:59Z 2008-04-11T23:03:21Z   0 0 09000064804506c5
FDA-2006-N-0236-0001 FDA Suicidality Data from Adult Antidepressant Trials FDA-2006-N-0236 FDA Notice NM-Notice of Meeting 2006-11-15T05:00:00Z 2006 11 2006-11-14T05:00:00Z 2006-12-02T04:59:59Z 2008-04-11T23:10:13Z   0 0 0900006480456a21
FDA-1988-N-0003-0006 FDA Prescription Drug Marketing Act of 1987; Guideline FDA-1988-N-0003 FDA Notice N-Notice 2006-11-15T05:00:00Z 2006 11 2006-11-14T05:00:00Z   2008-05-30T22:53:21Z   0 0 09000064804752dd
FDA-2006-N-0250-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Food Additive Petitions 21 CFR Part 571 ; Extension FDA-2006-N-0250 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Food Additive Petitions Notice General Notice 2006-11-15T05:00:00Z 2006 11 2006-11-15T05:00:00Z 2006-12-16T04:59:59Z 2025-06-30T16:19:05Z E6-19201 0 0 09000064804574ad
FDA-2006-N-0249-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602) FDA-2006-N-0249 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602) Notice General Notice 2006-11-15T05:00:00Z 2006 11 2006-11-15T05:00:00Z 2006-12-16T04:59:59Z 2025-06-30T16:06:21Z E6-19285 0 0 090000648045741e
FDA-2006-N-0252-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Agreement for Shipment of Devices for Sterilization FDA-2006-N-0252 Agency Information Collection Activities; Proposed Collection; Comment Request; Agreement for Shipment of Devices for Sterilization Notice General Notice 2006-11-15T05:00:00Z 2006 11 2006-11-15T05:00:00Z 2007-01-17T04:59:59Z 2025-07-08T20:13:41Z E6-19283 0 0 09000064804575a4
FDA-1992-N-0056-0018 FDA Prescription Drug Marketing Act of 1987, Drug Amds of 1992 FDA-1992-N-0056 Notice re Prescription Drug Marketing Act Pedigree Requirements under 21 CFR Part 203 Compliance Policy Guide and Guidance for Industry: Prescription Drug Marketing Act Pedigree Requirements Questions and Answers; Notice of Availability Notice General Notice 2006-11-15T05:00:00Z 2006 11 2006-11-14T05:00:00Z   2016-11-08T14:36:00Z   0 0 090000648052c00a
FDA-2006-D-0230-0001 FDA Draft Guidance for Industry: Protocols for the Conduct of Method Transfer Studies for Type C Medicated Feed Assay Methods Availability FDA-2006-D-0230 FDA Notice NAD-Notice of Availability of Data 2006-11-14T05:00:00Z 2006 11 2006-11-13T05:00:00Z 2007-01-30T04:59:59Z 2008-04-11T23:06:12Z   0 0 0900006480456323
FDA-2006-D-0302-0001 FDA Voluntary National Retail Food Regulatory Program Standards FDA-2006-D-0302 FDA Notice NAD-Notice of Availability of Data 2006-11-14T05:00:00Z 2006 11 2006-11-13T05:00:00Z 2007-01-17T04:59:59Z 2008-04-11T23:06:39Z   0 0 0900006480459166
FDA-2006-N-0426-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Medicated Feed Mill License Application 21 CFR Part 515 - Extension FDA-2006-N-0426 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Medicated Feed Mill License Application Notice General Notice 2006-11-14T05:00:00Z 2006 11 2006-11-14T05:00:00Z 2006-12-15T04:59:59Z 2025-06-30T17:01:19Z E6-19152 0 0 0900006480461a11
FDA-1992-N-0056-0017 FDA Prescription Drug Marketing Act of 1987, Drug Amds of 1992 FDA-1992-N-0056 Notice of Final Rule re Distribution of Blood Derivatives by Registered Blood Establishments Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Delay of Applicability Date Notice Notice of Final Rule 2006-11-13T05:00:00Z 2006 11 2006-11-09T05:00:00Z   2016-11-08T14:39:45Z   0 0 090000648052c009
FDA-2006-N-0184-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance on Reagents for Detection of Specific Novel Influenza A Viruses FDA-2006-N-0184 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Reagents for Detection of Specific Novel Influenza A Viruses Notice General Notice 2006-11-09T05:00:00Z 2006 11 2006-11-09T05:00:00Z 2006-12-12T04:59:59Z 2025-06-17T20:15:22Z E6-19045 0 0 0900006480450dce
FDA-2006-N-0251-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How To Use E-mail to Submit A Notice of Final Disposition Of Animals Not Intended For Immediate Slaughter FDA-2006-N-0251 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit a Notice of Final Disposition of Animals Not Intended for Immediate Slaughter Notice General Notice 2006-11-09T05:00:00Z 2006 11 2006-11-09T05:00:00Z 2007-01-09T04:59:59Z 2025-07-08T17:02:13Z E6-19044 0 0 0900006480457517
FDA-2006-N-0181-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-mail to Submit Information to the Center for Veterinary Medicine FDA-2006-N-0181 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit Information to the Center for Veterinary Medicine Notice General Notice 2006-11-08T05:00:00Z 2006 11 2006-11-08T05:00:00Z 2007-01-09T04:59:59Z 2025-07-08T16:48:07Z E6-18901 0 0 0900006480450d8a
FDA-2006-N-0114-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance For Industry On How To Use E-Mail To Submit A Request For A Meeting Or Teleconference To The Office Of New Animal Drug Evaluation FDA-2006-N-0114 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance For Industry on How to Use E-Mail to Submit a Request for a Meeting or Teleconference to the Office Of New Animal Drug Evaluation Notice General Notice 2006-11-08T05:00:00Z 2006 11 2006-11-08T05:00:00Z 2007-01-09T04:59:59Z 2025-07-08T17:51:42Z E6-18911 0 0 09000064804500ea
FDA-2006-N-0497-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit A Study Protocol FDA-2006-N-0497 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How To Use E-Mail To Submit A Study Protocol Notice General Notice 2006-11-08T05:00:00Z 2006 11 2006-11-08T05:00:00Z 2007-01-09T04:59:59Z 2025-07-08T18:57:50Z E6-18908 0 0 0900006480463868
FDA-2006-N-0182-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit a Notice of Intent to Slaughter for Human Food Purposes FDA-2006-N-0182 Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on How to Use E-Mail to Submit a Notice of Intent to Slaughter for Human Food Purposes Notice General Notice 2006-11-08T05:00:00Z 2006 11 2006-11-08T05:00:00Z 2007-01-09T04:59:59Z 2025-07-08T18:14:54Z E6-18896 0 0 0900006480450d98
FDA-2006-N-0494-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002 FDA-2006-N-0494 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002 Notice General Notice 2006-11-03T05:00:00Z 2006 11 2006-11-03T05:00:00Z 2006-12-05T04:59:59Z 2025-06-21T00:17:07Z E6-18603 0 0 090000648046377e
FDA-2006-N-0179-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Premarket Notification FDA-2006-N-0179 Agency Information Collection Activities; Proposed Collection; Comment Request; Premarket Notification Notice General Notice 2006-11-03T05:00:00Z 2006 11 2006-11-03T05:00:00Z 2007-01-03T04:59:59Z 2025-07-02T23:26:15Z E6-18553 0 0 0900006480450c0a
FDA-2004-N-0451-0010 FDA Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards FDA-2004-N-0451 Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 016 Notice Notice of Publication 2006-11-03T05:00:00Z 2006 11 2006-11-03T05:00:00Z   2025-04-16T16:00:40Z E6--18604 0 0 090000648047543b
FDA-2006-N-0228-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Reporting and Recordkeeping Requirements and Availability of Sample Electronic Products for Manufacturers and Distributors of Electronic Products FDA-2006-N-0228 Agency Information Collection Activities; Proposed Collection; Comment Request; Reporting and Recordkeeping Requirements and Availability of Sample Electronic Products for Manufacturers and Distributors of Electronic Products Notice General Notice 2006-11-03T05:00:00Z 2006 11 2006-11-03T05:00:00Z 2007-01-03T04:59:59Z 2025-07-02T23:46:12Z E6-18559 0 0 09000064804562d9
FDA-2006-N-0044-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device User Fee Cover Sheet FDA-2006-N-0044 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Medical Device User Fee Cover Sheet Notice General Notice 2006-11-03T05:00:00Z 2006 11 2006-11-03T05:00:00Z 2006-12-05T04:59:59Z 2025-06-18T23:34:36Z E6-18557 0 0 09000064804429c6
FDA-2005-D-0227-0004 FDA Questions and Answers Regarding Food Allergens, including the Food Allergen Labeling and Consumer Protection Act of 2004; Guidance (Edition 2) FDA-2005-D-0227 Questions and Answers Regarding Food Allergens, including the Food Allergen Labeling and Consumer Protection Act of 2004; Availability (Edition 4) Notice NAD-Notice of Availability of Data 2006-11-02T05:00:00Z 2006 11 2006-11-01T05:00:00Z 2007-11-02T03:59:59Z 2008-07-09T14:42:08Z   0 0 090000648044207c
FDA-2006-N-0180-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Substantial Evidence of Effectiveness of New Animal Drugs FDA-2006-N-0180 Agency Information Collection Activities; Proposed Collection; Comment Request; Substantial Evidence of Effectiveness of New Animal Drugs Notice General Notice 2006-11-02T05:00:00Z 2006 11 2006-11-02T05:00:00Z 2007-01-03T04:59:59Z 2025-07-03T01:10:23Z E6-18432 0 0 0900006480450cb5
FDA-2003-D-0030-0011 FDA Guidance on Marketed Unapproved Drugs Compliance Policy Guide FDA-2003-D-0030 FDA Notice NM-Notice of Meeting 2006-11-02T05:00:00Z 2006 11 2006-10-31T05:00:00Z   2008-04-12T00:54:01Z   0 0 0900006480481546
FDA-2006-N-0309-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; General Licensing Provisions: Biologics License Application, Changes to an Approved Application, Labeling, Revocation and Suspension, Postmarketing Studies Status Reports, and Forms FDA 356h and 2567 FDA-2006-N-0309 Agency Information Collection Activities; Proposed Collection; Comment Request; General Licensing Provisions: Biologics License Application, Changes to an Approved Application, Labeling, Revocation and Suspension, Postmarketing Studies Status Reports, and Forms FDA 356h and 2567 Notice General Notice 2006-11-02T05:00:00Z 2006 11 2006-11-02T05:00:00Z 2007-01-03T04:59:59Z 2025-07-02T23:58:42Z E6-18445 0 0 090000648045c6e8
FDA-2006-N-0306-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602) FDA-2006-N-0306 Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602) Notice General Notice 2006-10-31T05:00:00Z 2006 10 2006-10-31T05:00:00Z 2007-01-03T04:59:59Z 2025-07-02T23:38:35Z E6-18198 0 0 090000648045c57a
FDA-2006-N-0423-0003 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Infectious Disease Issues in Xenotransplantation FDA-2006-N-0423 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Infectious Disease Issues in Xenotransplantation Notice General Notice 2006-10-31T05:00:00Z 2006 10 2006-10-31T05:00:00Z 2006-12-01T04:59:59Z 2025-06-18T23:08:36Z E6-18203 0 0 09000064804618c5
FDA-2006-N-0489-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Investigational Device Exemptions Reports and Records FDA-2006-N-0489 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Investigational Device Exemptions Reports and Records Notice General Notice 2006-10-31T05:00:00Z 2006 10 2006-10-31T05:00:00Z 2006-12-01T04:59:59Z 2025-06-17T20:30:37Z E6-18200 0 0 090000648046356b
FDA-2006-D-0356-0001 FDA Guidance for Industry and Food and Drug Administration Staff; Draft Class II Special Controls Guidance Document: Absorbable Hemostatic Device FDA-2006-D-0356 Draft Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Absorbable Hemostatic Device; Availability Notice NAD-Notice of Availability of Data 2006-10-31T05:00:00Z 2006 10 2006-10-30T05:00:00Z 2007-01-30T04:59:59Z 2008-10-10T21:42:17Z   0 0 090000648045f6a0
FDA-2006-N-0417-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Administrative Detention and Banned Medical Devices FDA-2006-N-0417 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Administrative Detention and Banned Medical Devices Notice General Notice 2006-10-31T05:00:00Z 2006 10 2006-10-31T05:00:00Z 2006-12-01T04:59:59Z 2025-06-18T21:59:00Z E6-18190 0 0 0900006480461672
FDA-2006-N-0425-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Biological Products: Reporting of Biological Product Deviations in Manufacturing; Forms FDA 3486 and 3486A FDA-2006-N-0425 Agency Information Collection Activities; Proposed Collection; Comment Request; Biological Products: Reporting of Biological Product Deviations in Manufacturing; Forms FDA 3486 and 3486A Notice General Notice 2006-10-31T05:00:00Z 2006 10 2006-10-31T05:00:00Z 2007-01-03T04:59:59Z 2025-07-02T16:03:19Z E6-18313 0 0 0900006480461999
FDA-2004-D-0105-0009 FDA Guidance for Industry: Acceptable Full-Length Donor History Questionnaire and Accompanying Materials for Use in Screening Human Donors of Blood and Blood Components FDA-2004-D-0105 FDA Notice NAD-Notice of Availability of Data 2006-10-30T05:00:00Z 2006 10 2006-10-27T04:00:00Z 2007-10-31T03:59:59Z 2008-04-12T00:34:18Z   0 0 090000648046f5dc
FDA-2006-D-0297-0001 FDA Draft Guidance for Industry: Blue Bird Medicated Feed Labels; Availability FDA-2006-D-0297 Draft Guidance for Industry: Blue Bird Medicated Feed Labels; Availability Notice NAD-Notice of Availability of Data 2006-10-30T05:00:00Z 2006 10 2006-10-27T04:00:00Z 2007-01-17T04:59:59Z 2008-11-22T01:00:29Z   0 0 0900006480458df1
FDA-2006-N-0496-0001 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Orphan Drugs FDA-2006-N-0496 Agency Information Collection Activities; Proposed Collection; Comment Request; Orphan Drugs Notice General Notice 2006-10-29T04:00:00Z 2006 10 2006-10-30T05:00:00Z 2006-12-30T04:59:59Z 2025-07-01T23:32:05Z E6-18067 0 0 0900006480463820
FDA-2004-N-0054-0009 FDA Agency Information Collection Activities; Proposed Collection; MedWatch: The FDA Medical Products Reporting Program; Comment Request FDA-2004-N-0054 Agency Information Collection Activities; Announcement of Office of Management and Budget; Extension of Expiration Date for MedWatch (Food and Drug Administration Medical Products Reporting Program) Form Notice Notice of Extension 2006-10-26T04:00:00Z 2006 10     2025-06-05T19:12:02Z E6-17907 0 0 090000648046e914
FDA-2006-D-0039-0001 FDA Draft Guidance for Industry and Food and Drug Administration Staff; Annual Reports for Approved Premarket Approval Applications; Availability FDA-2006-D-0039 FDA Notice NAD-Notice of Availability of Data 2006-10-26T04:00:00Z 2006 10 2006-10-26T04:00:00Z 2007-01-25T04:59:59Z 2008-04-11T22:52:12Z   0 0 0900006480442261
FDA-2004-D-0299-0004 FDA Emergency Use Authorization of Medical Products FDA-2004-D-0299 FDA Notice NAL-Notice of Approval 2006-10-25T04:00:00Z 2006 10 2006-10-23T04:00:00Z   2008-04-12T00:35:41Z   0 0 0900006480472d3c
FDA-2006-D-0229-0001 FDA Guidance for Industry and FDA Staff: Total Product Life Cycle for Portable Invasive Blood Glucose Monitoring Systems FDA-2006-D-0229 FDA Notice NAD-Notice of Availability of Data 2006-10-25T04:00:00Z 2006 10 2006-10-23T04:00:00Z 2007-01-23T04:59:59Z 2008-04-11T23:06:11Z   0 0 09000064804562e3
FDA-2006-D-0360-0001 FDA Global Harmonization Task Force, Study Groups 1, 2, 4, and 5; New Proposed and Final Documents; Availability FDA-2006-D-0360 FDA Notice NAD-Notice of Availability of Data 2006-10-25T04:00:00Z 2006 10 2006-10-23T04:00:00Z 2007-01-23T04:59:59Z 2008-04-11T23:06:52Z   0 0 090000648045f966
FDA-2002-P-0226-0002 FDA Request for Rulemaking on Functional Foods & to Establish Advisory Committee FDA-2002-P-0226 FDA Notice - Notice of Hearing Before Commissioner Notice NHC-Notice of Hearing Before Commissioner 2006-10-25T04:00:00Z 2006 10 2006-10-24T04:00:00Z 2007-01-06T04:59:59Z 2009-03-18T22:03:17Z   0 0 090000648049746f
FDA-2006-F-0056-0001 FDA Safe Use of Cetylpyridinium Chloride as an Antimicrobial Agent in a Pre-chiller or Post-chiller Solution for Application to Raw Poultry Carcasses (FAP 6A4767) FDA-2006-F-0056 Safe Foods Corporation; Filing of Food Additive Petition Notice Notice of Filing 2006-10-25T04:00:00Z 2006 10 2006-10-25T04:00:00Z 2006-11-25T04:59:59Z 2026-01-10T08:06:50Z E6-17834 0 0 090000648044413b
FDA-2006-P-0074-0006 FDA To Exempt the Class II device Cranial Orthoses from Premarket Notification Requirements under section 510(m)(2)-CLOSED FDA-2006-P-0074 FDA Notice N-Notice 2006-10-25T04:00:00Z 2006 10 2006-10-23T04:00:00Z 2006-11-25T04:59:59Z 2008-04-11T23:17:40Z   0 0 09000064804445cf
FDA-2006-N-0493-0003 FDA Request for Samples and Protocols FDA-2006-N-0493 Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Request for Samples and Protocols Notice Notice of Approval 2006-10-25T00:00:00Z 2006 10 2006-10-24T04:00:00Z 2006-10-25T03:59:59Z 2025-05-17T00:02:01Z E6-17720 0 0 090000648046370a
FDA-2001-D-0008-0004 FDA Biological Product Deviation Reporting for Licensed Manufacturers FDA-2001-D-0008 FDA Notice NAD-Notice of Availability of Data 2006-10-20T04:00:00Z 2006 10 2006-10-19T04:00:00Z 2007-10-20T03:59:59Z 2008-04-25T02:25:09Z   0 0 09000064804b45d8
FDA-2001-D-0007-0003 FDA Biological Prod Deviation Reporting for Blood & Plasma Estab FDA-2001-D-0007 FDA Notice NAD-Notice of Availability of Data 2006-10-20T04:00:00Z 2006 10 2006-10-19T04:00:00Z 2007-10-20T03:59:59Z 2008-04-25T01:57:38Z   0 0 09000064804b443b
FDA-2004-D-0301-0006 FDA Guidance for Industry on Fixed Dose Combination and Co-Packaged Drug Products for Treatment of HIV' FDA-2004-D-0301 Guidance for Industry on Fixed Dose Combina.tions, Co-Packaged Drug Products, and Single-Entity Versions of Previously Approved Antiretrovirals for the Treatment of HIV; Availability Notice NAD-Notice of Availability of Data 2006-10-18T04:00:00Z 2006 10 2006-10-17T04:00:00Z 2007-10-19T03:59:59Z 2020-09-10T17:30:49Z   0 0 0900006480472ddf
FDA-2006-N-0474-0002 FDA Proposal to Debar for Anne L. Butkovitz, Notice of Opportunity for Hearing FDA-2006-N-0474 Anne L. Burkovitz; Debarment Order Notice Notice of Final Rule 2006-10-17T00:00:00Z 2006 10 2006-10-17T04:00:00Z 2006-10-18T03:59:59Z 2025-05-16T23:20:47Z E6-17178 1 0 0900006480462e7c
FDA-2006-N-0113-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Interstate Shellfish Dealers Certificate FDA-2006-N-0113 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Interstate Shellfish Dealers Certificate Notice General Notice 2006-10-13T04:00:00Z 2006 10 2006-10-13T04:00:00Z 2006-11-14T04:59:59Z 2025-06-16T23:25:54Z E6-16953 0 0 09000064804500df
FDA-1998-D-0019-0001 FDA Investigating out of Specification(OOS)Test Results fr Pharm FDA-1998-D-0019 FDA Notice NAD-Notice of Availability of Data 2006-10-12T04:00:00Z 2006 10 2006-10-11T04:00:00Z 2007-10-12T03:59:59Z 2008-05-16T21:17:59Z   0 0 0900006480563d59
FDA-2006-N-0307-0002 FDA Agency Information Collection Activities; Proposed Collection; Comment Request; Food Labeling; Trans Fatty Acids in Nutrition Labeling FDA-2006-N-0307 FDA Notice N-Notice 2006-10-12T00:00:00Z 2006 10 2006-10-11T00:00:00Z 2006-10-13T03:59:59Z 2025-05-07T01:19:39Z 71FR18338 0 0 090000648045c606
FDA-2004-E-0464-0006 FDA Patent Extension for BONIVA (ibandronate), U.S. Patent No. 4,927,814 FDA-2004-E-0464 Redetermination of Regulatory Review Period for Purposes of Patent Extension; BONIVA; Correction Notice Correction 2006-10-11T04:00:00Z 2006 10 2006-10-11T04:00:00Z   2025-11-20T18:32:10Z E6-16816 0 0 0900006480475801
FDA-2004-N-0189-0008 FDA Recordkeeping Requirements for Human Food and Cosmetics Manufactured from Processed With, or Otherwise Containing Material form Cattle FDA-2004-N-0189 RuleRecordkeeping Requirements for Human Food and Cosmetics Manufactured from Processed With, or Otherwise Containing Material form Cattle; Notice of Final Notice Notice of Final Rule 2006-10-11T04:00:00Z 2006 10 2006-10-10T04:00:00Z   2015-06-01T15:44:18Z   0 0 0900006480470948
FDA-2005-D-0023-0008 FDA Guidance for Industry on Bar Code Label Requirements; Questions and Answers FDA-2005-D-0023 FDA Notice NAD-Notice of Availability of Data 2006-10-10T04:00:00Z 2006 10 2006-10-04T04:00:00Z   2008-04-11T23:46:20Z   0 0 090000648043e7b9
FDA-2006-E-0124-0005 FDA Patent Extension Application for DRAXXIN (tulathromycin), U.S. Patent No. 6,420,536 FDA-2006-E-0124 Determination of Regulatory Review Period for Purposes of Patent Extension; DRAXXIN - Federal Register Notice Notice N-Notice 2006-10-03T04:00:00Z 2006 10 2006-09-29T04:00:00Z 2006-12-02T04:59:59Z 2008-05-30T16:45:01Z   0 0 09000064804501b5
FDA-2006-N-0112-0002 FDA Agency Information Collection Activities: Proposed Collection; Comment Request; Guidance for Industry Submitting and Reviewing Complete Responses to Clinical Holds FDA-2006-N-0112 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Proposed Collection; Comment Request; Guidance for Industry on Submitting and Reviewing Complete Responses to Clinical Holds Notice General Notice 2006-10-03T04:00:00Z 2006 10 2006-10-02T04:00:00Z 2006-11-02T04:59:59Z 2025-06-18T19:49:00Z E6-16225 0 0 09000064804500d0
FDA-2006-N-0419-0001 FDA Agency Information Collection Activities: Proposed Collection; Comment Request; Postmarket Surveillance FDA-2006-N-0419 Agency Information Collection Activities; Proposed Collection; Comment Request; Postmarket Surveillance Notice General Notice 2006-10-03T04:00:00Z 2006 10 2006-10-02T04:00:00Z 2006-12-02T04:59:59Z 2025-07-01T18:43:34Z E6-16231 0 0 0900006480461738
FDA-2006-E-0378-0005 FDA Patent Extension Application for BYETTA (exenatide injection), U.S. Patent No. 5,424,286 FDA-2006-E-0378 Determination of Regulatory Review Period for Purposes of Patent Extension; BYETTA Notice General Notice 2006-10-03T04:00:00Z 2006 10 2006-10-02T04:00:00Z   2025-12-18T00:32:20Z E6-16086 0 0 09000064804601b0
FDA-2006-N-0239-0002 FDA Index of Legally Marketed Unapproved New Animal Drugs for Minor Species FDA-2006-N-0239 Index of Legally Marketed Unapproved New Animal Drugs for Minor Species; Extension of Comment Period Notice Notice of Extension 2006-10-03T04:00:00Z 2006 10 2006-09-29T04:00:00Z 2006-12-21T04:59:59Z 2015-12-15T22:00:40Z   0 0 0900006480456f27

Next page

Advanced export

JSON shape: default, array, newline-delimited, object

CSV options: 

CREATE TABLE documents (
    id TEXT PRIMARY KEY,
    agency_id TEXT,
    docket_id TEXT REFERENCES dockets(id),
    title TEXT,
    document_type TEXT,
    subtype TEXT,
    posted_date TEXT,
    posted_year INTEGER,
    posted_month INTEGER,
    comment_start_date TEXT,
    comment_end_date TEXT,
    last_modified TEXT,
    fr_doc_num TEXT,
    open_for_comment INTEGER,
    withdrawn INTEGER,
    object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);