documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
241 rows where document_type = "Notice" and posted_year = 2001 sorted by posted_date descending
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| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| EPA-HQ-ORD-2004-0015-0002 | EPA | EPA-HQ-ORD-2004-0015 | Project Work Plan for Revised Air Quality Criteria for Ozone and Related Photochemical Oxidants | Notice | Federal Register Document | 2001-12-31T05:00:00Z | 2001 | 12 | 2001-12-31T05:00:00Z | 2002-02-16T04:59:59Z | 2010-07-15T19:14:49Z | 67524 | 0 | 0 | 09000064800c4bee |
| FDA-2001-N-0018-0001 | FDA | Preparation for ICH Meetings in Brussels, Belgium FDA-2001-N-0018 | Preparation for ICH Meetings in Brussels, Belgium, Including Progress on Implementation of the Common Technical Document; Notice of Public Meeting | Notice | General Notice | 2001-12-31T05:00:00Z | 2001 | 12 | 2025-02-10T16:52:56Z | 01-32123 | 0 | 0 | 09000064804b5107 | ||
| FDA-1978-N-0018-0441 | FDA | Sunscreen Drug Products -OPEN FDA-1978-N-0018 | Sunscreen Drug Products for Over-the-Counter Human Use; Final Monograph; Partial Stay; Final Rule | Notice | Notice of Stay of Action | 2001-12-31T05:00:00Z | 2001 | 12 | 2001-12-31T05:00:00Z | 2002-04-02T04:59:59Z | 2019-07-25T19:32:43Z | 01-32086 | 0 | 0 | 090000648055a801 |
| FDA-1993-D-0022-0001 | FDA | Microbiological Testing Antimicrobial Drug Residues in Foods FDA-1993-D-0022 | FDA | Notice | NAD-Notice of Availability of Data | 2001-12-31T05:00:00Z | 2001 | 12 | 2001-12-27T05:00:00Z | 2008-05-16T23:23:01Z | 0 | 0 | 09000064804face9 | ||
| FDA-2001-N-0015-0001 | FDA | Agency Information Collection; Customer/Partner Ser Surveys FDA-2001-N-0015 | Agency Information Collection Activities; Submission for OMB Review; Comment Request; Customer/Partner Service Surveys | Notice | 30 Day Proposed Information Collection | 2001-12-31T05:00:00Z | 2001 | 12 | 2001-12-20T05:00:00Z | 2002-01-23T04:59:59Z | 2025-01-17T16:28:25Z | 01-31335 | 0 | 0 | 09000064804b4d73 |
| EPA-HQ-RCRA-2001-0052-0001 | EPA | EPA-HQ-RCRA-2001-0052 | Proposed Collection, Comment Request, Final Authorization for Hazardous Waste Management, Information Collection Request Renewal | Notice | Federal Register Document | 2001-12-28T05:00:00Z | 2001 | 12 | 2008-01-08T21:20:08Z | 67245 | 0 | 0 | 09000064800e39f2 | ||
| FDA-2001-D-0223-0001 | FDA | Guidance on Labeling of Reprocessed Single Use Devices FDA-2001-D-0223 | FDA | Notice | N-Notice | 2001-12-28T05:00:00Z | 2001 | 12 | 2001-12-28T05:00:00Z | 2002-03-21T04:59:59Z | 2008-04-25T02:28:02Z | 0 | 0 | 09000064804e5374 | |
| FDA-2000-D-1403-0001 | FDA | Potassium Iodide as a Thyroid Blocking Agent FDA-2000-D-1403 | Potassium Iodide as a Thyroid Blocking Agent in Radiation Emergencies | Notice | Guidance | 2001-12-21T05:00:00Z | 2001 | 12 | 2021-10-01T04:00:00Z | 2002-12-12T04:59:59Z | 2024-11-07T21:53:19Z | 1 | 0 | 09000064804f0f7f | |
| EPA-HQ-OAR-2002-0003-0085 | EPA | Boutique Fuels -- White Paper ("Study of Unique Gasoline Fuel Blends ("Boutique Fuels''), Effects on Fuel Supply and Distribution and Potential Improvements'') Legacy Docket ID #: A-2001-20 EPA-HQ-OAR-2002-0003 | EPA Staff White Paper That Explores a Number of Options for Addressing Boutique Fuels in the Longer Term; Extension of Public Comment Period | Notice | Extension of Comment Period | 2001-12-19T05:00:00Z | 2001 | 12 | 2021-05-29T18:02:39Z | 01-31244 | 0 | 0 | 09000064800bca27 | ||
| EPA-HQ-RCRA-2002-0001-0025 | EPA | EPA-HQ-RCRA-2002-0001 | Solicitation of Proposals and Request for Comment, May 23, 1995, Final Rule | Notice | Federal Register Document | 2001-12-17T05:00:00Z | 2001 | 12 | 2008-01-08T21:15:47Z | 27282 | 0 | 0 | 09000064800df75b | ||
| EPA-HQ-RCRA-2002-0001-0008 | EPA | EPA-HQ-RCRA-2002-0001 | Regulatory Reinvention (XL) Pilot Projects; Project XL Draft Final Project Agreement: Waste Management, Inc. Landfill Bioreactor Systems, Notice of Availablity of U.S. Waste of Virginia, Inc., And King George Landfills, Inc. Final Project Agreement | Notice | Federal Register Document | 2001-12-17T05:00:00Z | 2001 | 12 | 2008-01-08T21:09:07Z | 54520 | 0 | 0 | 09000064800df6ef | ||
| EPA-HQ-RCRA-2002-0001-0022 | EPA | EPA-HQ-RCRA-2002-0001 | Alternate Liner Performance, Leachate Recirculation, And Bioreactor Landfills: Request for Information and Data | Notice | Federal Register Document | 2001-12-17T05:00:00Z | 2001 | 12 | 2008-01-08T21:11:31Z | 18014 | 0 | 0 | 09000064800df745 | ||
| EPA-HQ-RCRA-2002-0001-0027 | EPA | EPA-HQ-RCRA-2002-0001 | Notice of Modification to Project XL | Notice | Federal Register Document | 2001-12-17T05:00:00Z | 2001 | 12 | 2008-01-08T21:09:07Z | 19872 | 0 | 0 | 09000064800df768 | ||
| EPA-HQ-RCRA-2002-0001-0010 | EPA | EPA-HQ-RCRA-2002-0001 | Regulatory Reinvention (XL) Pilot Projects; Notice of Availability of Final Project Agreements and Related Documents | Notice | Federal Register Document | 2001-12-17T05:00:00Z | 2001 | 12 | 2008-01-08T21:17:57Z | 63250 | 0 | 0 | 09000064800df700 | ||
| EPA-HQ-RCRA-2002-0001-0026 | EPA | EPA-HQ-RCRA-2002-0001 | Regulatory Reinvention (XL) Pilot Projects; Solicitation of Proposals for and Request for Comment on Project XL | Notice | Federal Register Document | 2001-12-17T05:00:00Z | 2001 | 12 | 2008-01-08T21:17:57Z | 47929 | 0 | 0 | 09000064800df764 | ||
| FDA-2001-N-0172-0002 | FDA | Prescription Drug Product Labeling; Medication Guide Require FDA-2001-N-0172 | FDA | Notice | N-Notice | 2001-12-17T05:00:00Z | 2001 | 12 | 2001-12-17T05:00:00Z | 2002-01-15T04:59:59Z | 2008-04-25T02:27:22Z | 0 | 0 | 09000064804e0ae7 | |
| FDA-2001-N-0230-0002 | FDA | Prescription Drug User Fee Act (PDUFA) FDA-2001-N-0230 | FDA | Notice | NCR-Notice of Correction | 2001-12-07T05:00:00Z | 2001 | 12 | 2008-04-25T02:38:50Z | 0 | 0 | 09000064804e5d77 | |||
| FDA-2001-D-0040-0001 | FDA | Food-Effect Bioavailability & Fed Bioequivalence Studies FDA-2001-D-0040 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-29T05:00:00Z | 2001 | 11 | 2001-11-29T05:00:00Z | 2002-01-29T04:59:59Z | 2008-04-25T01:57:07Z | 0 | 0 | 09000064804b6d71 | |
| EPA-HQ-RCRA-2001-0041-0001 | EPA | EPA-HQ-RCRA-2001-0041 | Agency Information Collection Activities: Submission for OMB Review; Comment Request; Requirements for Generators, Transporters, and Hazardous Waste Management Facilities under the RCRA Hazardous Waste Manifest System, EPA ICR No. 801.14 | Notice | Federal Register Document | 2001-11-27T05:00:00Z | 2001 | 11 | 2001-11-27T05:00:00Z | 2002-01-29T04:59:59Z | 2008-01-08T21:20:56Z | 59248 | 0 | 0 | 09000064800e2b7b |
| FDA-2001-N-0070-0002 | FDA | Agency Information Collection Recall Regulations FDA-2001-N-0070 | Agency Information Collection Activities; Submission for OMB Review; Comment Request; FDA Recall Regulations | Notice | 30 Day Proposed Information Collection | 2001-11-27T05:00:00Z | 2001 | 11 | 2001-08-17T04:00:00Z | 2001-09-18T03:59:59Z | 2024-12-09T19:21:59Z | 01-20842 | 0 | 0 | 09000064804b825f |
| EPA-HQ-ORD-2004-0012-0020 | EPA | EPA-HQ-ORD-2004-0012 | Trichloroethylene Health Risk Assessment | Notice | Federal Register Document | 2001-11-26T05:00:00Z | 2001 | 11 | 2025-06-27T02:29:51Z | 59018 | 0 | 0 | 09000064800c4aa4 | ||
| FDA-2001-D-0032-0004 | FDA | Clinical Studies Section for Prescription Drugs & Biologics FDA-2001-D-0032 | FDA | Notice | NEC-Notice of Extension | 2001-11-21T05:00:00Z | 2001 | 11 | 2001-11-21T05:00:00Z | 2001-11-27T04:59:59Z | 2008-04-25T01:57:06Z | 0 | 0 | 09000064804b6347 | |
| FDA-2001-D-0219-0002 | FDA | Establishment & Operation of Clinical Trial Monitoring Comm FDA-2001-D-0219 | Draft Guidance for Clinical Trial Sponsors on the Establishment and Operation of Clinical Trial Data Monitoring Committees; Availability | Notice | NAD-Notice of Availability of Data | 2001-11-20T05:00:00Z | 2001 | 11 | 2001-11-19T05:00:00Z | 2002-02-20T04:59:59Z | 2010-05-10T16:34:55Z | 0 | 0 | 09000064804e4e02 | |
| FDA-1999-D-1301-0001 | FDA | Information Request & Discipline Review Letter FDA-1999-D-1301 | Guidance for Industry: Information Request & Discipline Review Letters Under the Prescription Drug User Fee Act | Notice | Guidance | 2001-11-20T05:00:00Z | 2001 | 11 | 2001-11-20T05:00:00Z | 2025-06-17T21:52:51Z | 1 | 0 | 09000064804da900 | ||
| FDA-2001-N-0230-0001 | FDA | Prescription Drug User Fee Act (PDUFA) FDA-2001-N-0230 | FDA | Notice | NM-Notice of Meeting | 2001-11-19T05:00:00Z | 2001 | 11 | 2001-11-19T05:00:00Z | 2002-01-26T04:59:59Z | 2008-04-25T02:38:50Z | 0 | 0 | 09000064804e5c39 | |
| FDA-1999-N-0053-0004 | FDA | Medical Devices; Reclassification of 38 Preamendments FDA-1999-N-0053 | FDA | Notice | NFR-Notice of Final Rule | 2001-11-16T05:00:00Z | 2001 | 11 | 2008-04-25T00:00:45Z | 0 | 0 | 09000064804a6196 | |||
| FDA-1999-N-0083-0001 | FDA | Assessment of Preclinical Reproductive Toxicity Data FDA-1999-N-0083 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-15T05:00:00Z | 2001 | 11 | 2001-11-15T05:00:00Z | 2002-03-14T04:59:59Z | 2008-04-25T00:00:59Z | 0 | 0 | 09000064804a6982 | |
| EPA-HQ-OAR-2002-0003-0084 | EPA | Boutique Fuels -- White Paper ("Study of Unique Gasoline Fuel Blends ("Boutique Fuels''), Effects on Fuel Supply and Distribution and Potential Improvements'') Legacy Docket ID #: A-2001-20 EPA-HQ-OAR-2002-0003 | Notice of Availability for Public Review and Comment of EPA Staff White Paper That Explores a Number of Options for Addressing Boutique Fuels | Notice | Federal Register Document | 2001-11-14T05:00:00Z | 2001 | 11 | 2021-05-25T01:00:38Z | 01-28522 | 0 | 0 | 09000064800bc9fe | ||
| FDA-2000-D-0196-0001 | FDA | Fumonisin Levels in Human Foods and Animal Feed FDA-2000-D-0196 | Guidance for Industry: Fumonisin Levels in Human Foods and Animal Feeds; Availability | Notice | Notice of Availability | 2001-11-14T05:00:00Z | 2001 | 11 | 2001-11-09T05:00:00Z | 2002-11-10T04:59:59Z | 2018-10-10T18:41:38Z | 0 | 0 | 09000064804d4563 | |
| FDA-2001-D-0137-0002 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb03 | |
| FDA-2001-D-0137-0007 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb0b | |
| FDA-2001-N-0176-0001 | FDA | Inhalational Anthrax (Post-Exposure) Doxycycline/PenicillinG FDA-2001-N-0176 | FDA | Notice | N-Notice | 2001-11-06T05:00:00Z | 2001 | 11 | 2008-04-25T02:27:33Z | 0 | 0 | 09000064804e1102 | |||
| FDA-2001-N-0176-0002 | FDA | Inhalational Anthrax (Post-Exposure) Doxycycline/PenicillinG FDA-2001-N-0176 | FDA | Notice | N-Notice | 2001-11-06T05:00:00Z | 2001 | 11 | 2008-04-25T02:27:34Z | 0 | 0 | 09000064804e133a | |||
| FDA-2001-D-0137-0001 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddaef | |
| FDA-2001-N-0074-0002 | FDA | Withdrawal of 51 NDAs and 25 ANDAs FDA-2001-N-0074 | Schering Corp. et al.; Withdrawal of Approval of 51 New Drug Applications and 25 Abbreviated New Drug Applications; Correction | Notice | Correction | 2001-11-06T05:00:00Z | 2001 | 11 | 2025-01-29T14:22:16Z | 01-27520 | 0 | 0 | 09000064804b831d | ||
| FDA-2001-D-0137-0006 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb0a | |
| FDA-2001-D-0137-0009 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb0d | |
| FDA-2001-D-0137-0008 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb0c | |
| FDA-2001-N-0074-0003 | FDA | Withdrawal of 51 NDAs and 25 ANDAs FDA-2001-N-0074 | Schering Corp. et al.; Withdrawal of Approval of 51 New Drug Applications and 25 Abbreviated New Drug Applications; Correction | Notice | Correction | 2001-11-06T05:00:00Z | 2001 | 11 | 2025-01-29T14:37:32Z | 01-27520 | 0 | 0 | 09000064804b831e | ||
| FDA-2001-D-0137-0003 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb05 | |
| FDA-2001-D-0137-0005 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb09 | |
| FDA-2001-D-0137-0004 | FDA | Evalution of the effects of Orally Inhaled and Intranasal FDA-2001-D-0137 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-06T05:00:00Z | 2001 | 11 | 2001-11-06T05:00:00Z | 2002-02-05T04:59:59Z | 2008-04-25T02:25:55Z | 0 | 0 | 09000064804ddb08 | |
| FDA-2001-D-0219-0001 | FDA | Establishment & Operation of Clinical Trial Monitoring Comm FDA-2001-D-0219 | Draft FDA Guidance on the Estabtishment and Operation of Clinical Trial Data Monitoring Committees; Public Meeting | Notice | NM-Notice of Meeting | 2001-11-05T05:00:00Z | 2001 | 11 | 2010-05-10T16:33:19Z | 0 | 0 | 09000064804e4d7b | |||
| FDA-2001-N-0016-0001 | FDA | Veterinary adverse drug reaction, lack of effect, product FDA-2001-N-0016 | Agency Information Collection Activities; Submission for OMB Review; Comment Request; Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report | Notice | 30 Day Proposed Information Collection | 2001-11-05T05:00:00Z | 2001 | 11 | 2001-11-05T05:00:00Z | 2001-12-06T04:59:59Z | 2024-12-17T02:00:53Z | 01-27641 | 0 | 0 | 09000064804b4ea8 |
| FDA-2001-N-0171-0001 | FDA | Medical Devices: Third-Party review under FDAMA;Agency Infor FDA-2001-N-0171 | Agency Information Collection Activities; Announcement of OMB Approval; Third-Party Review Under FDAMA | Notice | Notice of Approval | 2001-11-05T05:00:00Z | 2001 | 11 | 2024-12-16T17:04:30Z | 01-27642 | 0 | 0 | 09000064804e0921 | ||
| FDA-2000-D-0027-0001 | FDA | Patulin in Apple Juice,Apple Juice Concentrates,Juice Produc FDA-2000-D-0027 | FDA | Notice | NAD-Notice of Availability of Data | 2001-11-05T05:00:00Z | 2001 | 11 | 2008-04-25T01:01:00Z | 0 | 0 | 09000064804aeaf2 | |||
| EPA-HQ-OECA-2005-0006-0003 | EPA | Clean Water Act Class II: Proposed Administrative Settlement, Penalty Assessment and Opportunity to Comment Regarding Standard Steel, a Division of Freedom Forge Corporation EPA-HQ-OECA-2005-0006 | Clean Water Act Class II: Proposed Administrative Settlement, Penalty Assessment and Opportunity To Comment Regarding Standard Steel, a Division of Freedom Forge Corporation; Extension of Comment Period [III-A-003] | Notice | Federal Register Document | 2001-10-30T05:00:00Z | 2001 | 10 | 2001-10-30T05:00:00Z | 2001-11-10T04:59:59Z | 2010-07-15T19:13:40Z | 54770 | 0 | 0 | 09000064800b88c8 |
| FDA-1998-N-0050-0002 | FDA | Comprehensive List of Current Guidance Documents at FDA FDA-1998-N-0050 | Annual Comprehensive List of Guidance Documents at the Food and Drug Administration | Notice | General Notice | 2001-10-29T05:00:00Z | 2001 | 10 | 2001-10-24T04:00:00Z | 2015-04-11T02:07:31Z | 0 | 0 | 090000648056e813 | ||
| FDA-2001-N-0174-0001 | FDA | Electronic Interchange Standard for Digital ECG; Public Meet FDA-2001-N-0174 | Electronic Interchange Standard for Digital ECG and Similar Data; Public Meeting | Notice | Meeting | 2001-10-29T05:00:00Z | 2001 | 10 | 2025-02-06T02:00:57Z | 01-26821 | 0 | 0 | 09000064804e0d65 | ||
| FDA-2001-N-0201-0001 | FDA | Food Labeling; Notification Procedures on Dietary Supplement FDA-2001-N-0201 | Agency Information Collection Activities; Proposed Collection; Comment Request; Food Labeling; Notification Procedures for Statements on Dietary Supplements | Notice | 60 Day Proposed Information Collection | 2001-10-29T05:00:00Z | 2001 | 10 | 2025-02-04T17:06:58Z | 01-26885 | 0 | 0 | 09000064804e35f6 | ||
| FDA-1999-F-0120-0003 | FDA | Listed Gum or Wood Rosin Derivatives FDA-1999-F-0120 | Food Additives Permitted for Direct Addition to Food for Human Consumption; Change in Specifications for Gum or Wood Rosin Derivatives in Chewing Gum Base; Correction | Notice | Correction | 2001-10-29T00:00:00Z | 2001 | 10 | 2025-05-02T18:20:56Z | 01-26708 | 0 | 0 | 09000064804ae961 | ||
| FDA-2001-N-0199-0001 | FDA | Premarket Notification 510(k) Submissions FDA-2001-N-0199 | Agency Information Collection Activities; Announcement of OMB Approval; Premarket Notification 510(k) Submissions | Notice | Notice of Approval | 2001-10-26T04:00:00Z | 2001 | 10 | 2024-12-10T16:05:25Z | 01-26573 | 0 | 0 | 09000064804e3357 | ||
| FDA-2001-D-0094-0002 | FDA | Channels of trade policy for Commodities with Vinclozolin FDA-2001-D-0094 | FDA | Notice | N-Notice | 2001-10-23T04:00:00Z | 2001 | 10 | 2001-10-23T04:00:00Z | 2001-11-24T04:59:59Z | 2008-04-25T02:23:58Z | 0 | 0 | 09000064804b90d5 | |
| FDA-2001-N-0104-0001 | FDA | Fast Track Drug Development Programs: Designation, Development, and Application Review FDA-2001-N-0104 | Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry: Fast Track Drug Development Programs-Designation, Development, and Application Review | Notice | 60 Day Proposed Information Collection | 2001-10-23T04:00:00Z | 2001 | 10 | 2001-10-23T04:00:00Z | 2001-12-25T04:59:59Z | 2025-02-03T20:03:20Z | 01-26575 | 0 | 0 | 09000064804bae60 |
| FDA-1980-N-0074-0074 | FDA | Anticaries Drug Products for OTC Human Use; FDA-1980-N-0074 | FDA | Notice | N-Notice | 2001-10-22T04:00:00Z | 2001 | 10 | 2001-10-22T04:00:00Z | 2002-01-15T04:59:59Z | 2008-05-30T22:53:09Z | 0 | 0 | 09000064805bb4da | |
| FDA-2001-N-0170-0001 | FDA | Medical Device Labeling Regulations FDA-2001-N-0170 | Agency Information Collection Activities; Submission for OMB Review; Comment Request; Medical Device Labeling Regulations | Notice | 30 Day Proposed Information Collection | 2001-10-19T04:00:00Z | 2001 | 10 | 2001-10-16T04:00:00Z | 2001-11-16T04:59:59Z | 2024-12-19T19:57:40Z | 01-25943 | 0 | 0 | 09000064804e07d0 |
| FDA-2001-N-0566-0001 | FDA | New Animal Drugs for Investigational;Agency Information Coll FDA-2001-N-0566 | Agency Information Collection Activities; Proposed Collection; Comment Request; New Animal Drugs for Investigational Use | Notice | 60 Day Proposed Information Collection | 2001-10-19T04:00:00Z | 2001 | 10 | 2001-10-16T04:00:00Z | 2001-12-18T04:59:59Z | 2025-02-03T18:49:59Z | 01-25918 | 0 | 0 | 090000648050b0cb |
| EPA-HQ-RCRA-2001-0008-0011 | EPA | EPA-HQ-RCRA-2001-0008 | Notice of Availability of the Draft Guidance on Demonstrating Compliance With the Land Disposal Restrictions Alternative Soil Treatment Standards, and the Draft Interpretative Memorandum on the Stabilization of Organic-Bearing Hazardous Wastes [F-2001-DRG2-FFFFF] | Notice | Federal Register Document | 2001-10-18T04:00:00Z | 2001 | 10 | 2001-10-18T04:00:00Z | 2001-12-04T04:59:59Z | 2008-01-08T21:09:42Z | 52918 | 0 | 0 | 09000064800def81 |
| EPA-HQ-RCRA-2001-0050-0084 | EPA | EPA-HQ-RCRA-2001-0050 | National Recommended Water Quality Criteria; Republication; Compilation of Recommended Water Quality Criteria and Notice of Process for New and Revised Criteria | Notice | Federal Register Document | 2001-10-15T04:00:00Z | 2001 | 10 | 2008-01-08T21:11:36Z | 68354 | 0 | 0 | 09000064800e35e2 | ||
| EPA-HQ-OECA-2005-0005-0003 | EPA | Clean Water Act Class II: Proposed Administrative Settlement, Penalty Assessment and Opportunity to Comment Regarding WorldCom, Inc. EPA-HQ-OECA-2005-0005 | Corrected Federal Register Notice for original Federal Register which is document number OECA-2005-0005-0002 [III-A-002] | Notice | Federal Register Document | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2001-11-14T04:59:59Z | 2010-07-15T19:13:40Z | 52135 | 0 | 0 | 09000064800b8854 |
| EPA-HQ-RCRA-2001-0007-0006 | EPA | EPA-HQ-RCRA-2001-0007 | Notice of the Availability of the Draft Guidance in Demonstrating Compliance with the Land Disposal Restrictions Alternative Soil Treatment Standards, and the Draft Interpretative Memorandum on the Stabilization of Organic-Bearing Hazardous Wastes [F-2001-DRG1-FFFFF] | Notice | Federal Register Document | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2001-12-04T04:59:59Z | 2022-04-21T01:00:44Z | 52918 | 0 | 0 | 09000064800def23 |
| FDA-1998-D-0037-0001 | FDA | Format for Geriatric Labeling FDA-1998-D-0037 | FDA | Notice | NAD-Notice of Availability of Data | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2002-10-06T03:59:59Z | 2008-05-16T21:18:13Z | 0 | 0 | 0900006480565bc6 | |
| FDA-2000-D-0100-0002 | FDA | Clinical Data In Marketing Applications FDA-2000-D-0100 | FDA | Notice | NAD-Notice of Availability of Data | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2002-10-06T03:59:59Z | 2008-04-25T01:47:25Z | 0 | 0 | 09000064804c217b | |
| FDA-2000-P-0102-0004 | FDA | Health Claim: Vegetable Oil Sterol Esters & Coronary Heart Disease CLOSED 05/26/2020 FDA-2000-P-0102 | FDA | Notice | NEC-Notice of Extension | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2001-11-20T04:59:59Z | 2008-04-25T01:47:38Z | 0 | 0 | 09000064804c22da | |
| FDA-2000-P-0133-0004 | FDA | Health Claim: Plant Stanol Esters and Heart Disease CLOSED 05/26/2020 FDA-2000-P-0133 | FDA | Notice | NEC-Notice of Extension | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2001-11-20T04:59:59Z | 2008-04-25T01:16:05Z | 0 | 0 | 09000064804cfd51 | |
| FDA-1998-D-0037-0002 | FDA | Format for Geriatric Labeling FDA-1998-D-0037 | FDA | Notice | NAD-Notice of Availability of Data | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2002-10-06T03:59:59Z | 2008-05-16T21:18:13Z | 0 | 0 | 0900006480565c35 | |
| FDA-2001-N-0068-0001 | FDA | GLP Regulations for Nonclinical Laboratory Studies FDA-2001-N-0068 | Agency Information Collection Activities; Announcement of OMB Approval; Good Laboratory Practices (GLP) Regulations for Nonclinical Laboratory Studies | Notice | Notice of Approval | 2001-10-12T04:00:00Z | 2001 | 10 | 2025-02-11T16:56:25Z | 01-25659 | 0 | 0 | 09000064804b81dc | ||
| FDA-2001-N-0226-0002 | FDA | Reports of Corrections and Removals:Agency Information Colle FDA-2001-N-0226 | Agency Information Collection Activities; Submission for OMB Review; Comment Request; Reports of Corrections and Removals | Notice | 30 Day Proposed Information Collection | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-12T04:00:00Z | 2001-11-14T04:59:59Z | 2025-01-15T20:59:09Z | 01-25660 | 0 | 0 | 09000064804e57a8 |
| FDA-2001-N-0072-0001 | FDA | CGMP Regulations for Type A Medicated Articles FDA-2001-N-0072 | Agency Information Collection Activities; Announcement of OMB Approval; Current Good Manufacturing Practice Regulations for Type A Medicated Articles | Notice | Notice of Approval | 2001-10-12T04:00:00Z | 2001 | 10 | 2024-11-26T02:00:30Z | 01-25658 | 0 | 0 | 09000064804b82d8 | ||
| FDA-2001-N-0105-0001 | FDA | Third-Party Submissions review/quality system inspections FDA-2001-N-0105 | Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Devices; Third-Party Premarket Submission Review and Quality System Inspections Under United States/European Community Mutual Recognition Agreement | Notice | 60 Day Proposed Information Collection | 2001-10-12T04:00:00Z | 2001 | 10 | 2001-10-05T04:00:00Z | 2001-12-05T04:59:59Z | 2025-01-31T16:15:35Z | 01-24998 | 0 | 0 | 09000064804bafb0 |
| EPA-HQ-RCRA-2002-0004-0001 | EPA | EPA-HQ-RCRA-2002-0004 | Notice of the Availability; The Office of Solid Waste Announces the Availability of a New Guidance Document; Risk Burn Guidance for Hazardous Waste Combustion Facitities (Supporting Materials are in the File for the Draft Guidance, (F-1998-GCEA-FFFFF) | Notice | Federal Register Document | 2001-10-11T04:00:00Z | 2001 | 10 | 2008-01-08T21:17:57Z | 51953 | 0 | 0 | 09000064800dfa6e | ||
| EPA-HQ-RCRA-2001-0028-0001 | EPA | EPA-HQ-RCRA-2001-0028 | Agency Information Collection Activities Up for Renewal: Comment Request; State Program Adequacy Determination | Notice | Federal Register Document | 2001-10-11T04:00:00Z | 2001 | 10 | 2001-10-11T04:00:00Z | 2001-12-11T04:59:59Z | 2008-01-08T21:12:21Z | 51949 | 0 | 0 | 09000064800e1a11 |
| FDA-2000-D-0068-0001 | FDA | Electronic Signatures: Glossary of Terms FDA-2000-D-0068 | FDA | Notice | NCR-Notice of Correction | 2001-10-11T04:00:00Z | 2001 | 10 | 2008-04-25T01:13:24Z | 0 | 0 | 09000064804afe17 | |||
| EPA-HQ-OECA-2005-0006-0002 | EPA | Clean Water Act Class II: Proposed Administrative Settlement, Penalty Assessment and Opportunity to Comment Regarding Standard Steel, a Division of Freedom Forge Corporation EPA-HQ-OECA-2005-0006 | Corrected Federal Register Notice for original Federal Register which is document number OECA-2005-0006-0001 [III-A-002] | Notice | Federal Register Document | 2001-10-10T04:00:00Z | 2001 | 10 | 2001-10-10T04:00:00Z | 2001-10-30T04:59:59Z | 2010-07-15T19:13:40Z | 51667 | 0 | 0 | 09000064800b88b9 |
| FDA-2001-N-0202-0002 | FDA | Workshop on Preclinical Testing for Endovascular Grafts FDA-2001-N-0202 | Workshop on Preclinical Testing for Endovascular Grafts | Notice | NM-Notice of Meeting | 2001-10-10T04:00:00Z | 2001 | 10 | 2009-01-07T16:52:55Z | 0 | 0 | 09000064804e3787 | |||
| FDA-2001-N-0202-0001 | FDA | Workshop on Preclinical Testing for Endovascular Grafts FDA-2001-N-0202 | Workshop on Preclinical Testing for Endovascular Grafts | Notice | NM-Notice of Meeting | 2001-10-10T04:00:00Z | 2001 | 10 | 2009-01-07T16:51:36Z | 01–16471 | 0 | 0 | 09000064804e373f | ||
| FDA-2001-N-0567-0001 | FDA | Substances Prohibited from use in animal food/Feed Ruminant FDA-2001-N-0567 | FDA | Notice | NH-Notice of Hearing | 2001-10-10T04:00:00Z | 2001 | 10 | 2008-04-25T02:39:30Z | 0 | 0 | 090000648050b0de | |||
| FDA-2001-N-0047-0002 | FDA | Progress on implementing for the common technical document FDA-2001-N-0047 | Preparation for ICH Meetings in Brussels, Belgium, Including Progress on Implementing of the Common Technical Document; Public Meeting; Cancellation | Notice | General Notice | 2001-10-02T04:00:00Z | 2001 | 10 | 2025-01-30T19:01:03Z | 01-24528 | 0 | 0 | 09000064804b78ae | ||
| EPA-HQ-RCRA-2003-0018-0001 | EPA | EPA-HQ-RCRA-2003-0018 | Agency Information Collection Activities: Submission for OMB Review; Comment Request; Criteria for Classification of Solid Waste Disposal Facilities and Practices, Recordkeeping and Reporting Requirements; 40 CFR Part 257, Subpart B; Notice | Notice | Federal Register Document | 2001-10-01T04:00:00Z | 2001 | 10 | 2001-10-01T04:00:00Z | 2002-11-01T04:59:59Z | 2008-01-08T21:13:35Z | 61621 | 0 | 0 | 09000064800e3822 |
| FDA-2001-P-0005-0001 | FDA | Determination that Disulfiram was withdrawn for reasons othe FDA-2001-P-0005 | Notice of Determination | Notice | N-Notice | 2001-10-01T04:00:00Z | 2001 | 10 | 2024-08-28T13:26:37Z | 0 | 0 | 09000064804b4014 | |||
| FDA-2001-N-0173-0001 | FDA | Rapid Response Surveys;Agency Information Collection FDA-2001-N-0173 | Agency Information Collection Activities; Proposed Collection; Comment Request; Rapid Response Surveys | Notice | 60 Day Proposed Information Collection | 2001-10-01T04:00:00Z | 2001 | 10 | 2001-09-27T04:00:00Z | 2001-11-27T04:59:59Z | 2025-01-30T21:09:38Z | 01-24163 | 0 | 0 | 09000064804e0bdd |
| FDA-1998-D-0037-0003 | FDA | Format for Geriatric Labeling FDA-1998-D-0037 | Content and Format for Geriatric Labeling | Notice | Guidance | 2001-10-01T04:00:00Z | 2001 | 10 | 2001-10-01T04:00:00Z | 2021-10-01T04:02:28Z | 0 | 0 | 0900006480565c32 | ||
| EPA-HQ-OECA-2005-0006-0001 | EPA | Clean Water Act Class II: Proposed Administrative Settlement, Penalty Assessment and Opportunity to Comment Regarding Standard Steel, a Division of Freedom Forge Corporation EPA-HQ-OECA-2005-0006 | Clean Water Act Class II: Proposed Administrative Settlement, Penalty Assessment and Opportunity to Comment Regarding Standard Steel, a Division of Freedom Forge Corporation [III-A-001] | Notice | Federal Register Document | 2001-09-27T04:00:00Z | 2001 | 9 | 2001-09-27T04:00:00Z | 2001-10-30T04:59:59Z | 2010-07-15T19:13:40Z | 49379 | 0 | 0 | 09000064800b88a4 |
| FDA-2000-D-0002-0003 | FDA | Q7A ICH Good Manufacturing Practice Guide for Active Pharmaceuticals FDA-2000-D-0002 | FDA | Notice | NAD-Notice of Availability of Data | 2001-09-26T04:00:00Z | 2001 | 9 | 2008-04-25T01:13:52Z | 0 | 0 | 09000064804ae5c1 | |||
| FDA-2001-N-0172-0001 | FDA | Prescription Drug Product Labeling; Medication Guide Require FDA-2001-N-0172 | FDA | Notice | N-Notice | 2001-09-26T04:00:00Z | 2001 | 9 | 2001-09-26T04:00:00Z | 2001-11-27T04:59:59Z | 2008-04-25T02:27:22Z | 0 | 0 | 09000064804e0a96 | |
| FDA-2001-D-0164-0001 | FDA | Guidance ICH Q1D Bracketing and Matrixing Designs for Stabil FDA-2001-D-0164 | FDA | Notice | NAD-Notice of Availability of Data | 2001-09-26T04:00:00Z | 2001 | 9 | 2001-09-26T04:00:00Z | 2001-11-27T04:59:59Z | 2008-04-25T02:27:39Z | 0 | 0 | 09000064804dff39 | |
| FDA-2001-N-0175-0001 | FDA | Transportation Safety & Potentially Sedating or Impairing FDA-2001-N-0175 | Meeting on 11/14-15/01 | Notice | NM-Notice of Meeting | 2001-09-24T04:00:00Z | 2001 | 9 | 2001-09-24T04:00:00Z | 2001-12-18T04:59:59Z | 2008-04-25T02:27:52Z | 0 | 0 | 09000064804e0ed7 | |
| FDA-2000-D-0031-0001 | FDA | Electronic Records; Electronic Signatures, Validation FDA-2000-D-0031 | FDA | Notice | NAD-Notice of Availability of Data | 2001-09-24T04:00:00Z | 2001 | 9 | 2001-09-24T04:00:00Z | 2001-12-25T04:59:59Z | 2008-04-25T01:12:34Z | 0 | 0 | 09000064804aeb8d | |
| FDA-2001-E-0151-0001 | FDA | Patent Extension for Trileptal, No. 4,559,174 FDA-2001-E-0151 | Determination of Regulatory Review Period for Purposes of Patent Extension; Trileptal | Notice | General Notice | 2001-09-24T04:00:00Z | 2001 | 9 | 2001-09-24T04:00:00Z | 2001-11-24T04:59:59Z | 2025-09-15T16:10:58Z | 0 | 0 | 09000064804ddd1d | |
| FDA-2000-E-0239-0001 | FDA | Patent Extension Synercid #4,668,669 FDA-2000-E-0239 | Determination of Regulatory Review Period for Purposes of Patent Extension; Synercid | Notice | General Notice | 2001-09-21T04:00:00Z | 2001 | 9 | 2001-09-21T04:00:00Z | 2002-03-21T04:59:59Z | 2025-07-09T16:09:54Z | 0 | 0 | 09000064804d59f6 | |
| FDA-2001-E-0210-0001 | FDA | Kaletra, Patent Extension Application No.5,886,036 FDA-2001-E-0210 | Determination of Regulatory Review Period for Purposes of Patent Extension; Kaletra | Notice | General Notice | 2001-09-21T04:00:00Z | 2001 | 9 | 2001-09-21T04:00:00Z | 2002-03-21T04:59:59Z | 2025-10-01T18:13:42Z | 0 | 0 | 09000064804e41c2 | |
| FDA-2001-F-0180-0001 | FDA | use of mixture of peroxyacetic acid,octanoic acid,acetic FDA-2001-F-0180 | Secondary Direct Food Additives Permitted in Food for Human Consumption | Notice | Notice of Final Rule | 2001-09-21T04:00:00Z | 2001 | 9 | 2001-09-21T04:00:00Z | 2001-10-20T03:59:59Z | 2025-11-06T20:46:42Z | 0 | 0 | 09000064804e1878 | |
| FDA-2001-E-0234-0001 | FDA | Rescula, Patent Extension Application No. 5,221,763 FDA-2001-E-0234 | Determination of Regulatory Review Period for Purposes of Patent Extension; Rescula | Notice | General Notice | 2001-09-21T04:00:00Z | 2001 | 9 | 2001-09-21T04:00:00Z | 2002-03-21T04:59:59Z | 2025-10-10T22:02:07Z | 0 | 0 | 09000064804e6296 | |
| EPA-HQ-ORD-2004-0012-0001 | EPA | EPA-HQ-ORD-2004-0012 | Trichloroethylene Health Risk Assessment | Notice | Federal Register Document | 2001-09-19T04:00:00Z | 2001 | 9 | 2025-06-27T02:26:44Z | 58257 | 0 | 0 | 09000064800c49bb | ||
| FDA-1996-P-0025-0001 | FDA | Reduce the Precense of Salmonella Enteritidis in Shell Eggs - CLOSED FDA-1996-P-0025 | FDA | Notice | Notice of Availability | 2001-09-18T04:00:00Z | 2001 | 9 | 2001-09-18T04:00:00Z | 2002-09-08T03:59:59Z | 2016-05-31T16:17:22Z | 0 | 0 | 09000064804faaa3 | |
| FDA-1998-N-0087-0001 | FDA | Labeling of Shell Eggs;Shell Eggs: Refrigeration of Shell FDA-1998-N-0087 | FDA | Notice | NAD-Notice of Availability of Data | 2001-09-18T04:00:00Z | 2001 | 9 | 2001-09-18T04:00:00Z | 2002-09-08T03:59:59Z | 2008-05-16T21:37:51Z | 0 | 0 | 0900006480585263 | |
| FDA-1994-P-0050-0002 | FDA | Amend Reference Amount for Baking Soda to read 1/8 tsp FDA-1994-P-0050 | FDA | Notice | NAD-Notice of Availability of Data | 2001-09-18T04:00:00Z | 2001 | 9 | 2001-09-18T04:00:00Z | 2002-09-08T03:59:59Z | 2008-05-16T23:21:35Z | 0 | 0 | 09000064804ffa38 | |
| FDA-1997-P-0017-0002 | FDA | Require that warning labels about risks of salmonella enteri FDA-1997-P-0017 | Notice of Availability of Data re Small Entity Compliance Guide: “Food Labeling: Safe Handling Statements, Labeling of Shell Eggs; Refrigeration of Shell Eggs Held for Retail Distribution;” Availability | Notice | Notice of Data Availability | 2001-09-18T04:00:00Z | 2001 | 9 | 2001-09-18T04:00:00Z | 2002-09-08T03:59:59Z | 2015-05-12T15:29:10Z | 0 | 0 | 09000064805c9fc0 | |
| FDA-2001-N-0047-0001 | FDA | Progress on implementing for the common technical document FDA-2001-N-0047 | Preparation for ICH Meetings in Brussels, Belgium, Including Progress on Implementing of the Common Technical Document; Public Meeting | Notice | Meeting | 2001-09-12T04:00:00Z | 2001 | 9 | 2025-01-30T17:36:45Z | 01-22471 | 0 | 0 | 09000064804b78a3 | ||
| FDA-2001-N-0133-0002 | FDA | Exemption From Premarket Notification Requirements; Class 1 FDA-2001-N-0133 | Medical Devices; Exemption From Premarket Notification Requirements; Class I Devices | Notice | Correction | 2001-09-10T04:00:00Z | 2001 | 9 | 2025-02-11T15:27:21Z | 01-22577 | 0 | 0 | 09000064804dda85 |
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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);