dockets: APHIS-2021-0062

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

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id agency_id title docket_type last_modified object_id rin dkabstract category subtype keywords program short_title effective_date organization attrs_raw attr_source
APHIS-2021-0062 APHIS Draft Guidance for Requesting a Regulatory Status Review under 7 CFR part 340 Nonrulemaking 2021-10-28T08:48:25Z 0b00006484c78e06   The revised biotechnology regulations in 7 CFR part 340 identify high-level information requirements for submissions of Regulatory Status Review (RSR) requests for plants developed using genetic engineering, and state that detailed information on how to meet the information requirements can be found on the APHIS website (§340.4(a)(4)). APHIS is publishing a Draft Regulatory Status Review Guide to provide more detailed information on how to prepare a submission for Regulatory Status Review. This Draft Regulatory Status Review Guide will be available for public review and comment beginning August 25, 2021, and ending October 25, 2021. If you wish to view the document and submit a comment, click on the "Browse & Comment on Documents" link. Genetically Modified Organisms and Products   ["USDA", "agriculture"] Biotechnology Regulatory Services       {"displayProperties": [{"name": "abstract", "label": "Summary", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, General Info, Summary."}], "keywords": ["USDA", "agriculture"], "modifyDate": "2021-10-28T08:48:25Z", "dkAbstract": "The revised biotechnology regulations in 7 CFR part 340 identify high-level information requirements for submissions of Regulatory Status Review (RSR) requests for plants developed using genetic engineering, and state that detailed information on how to meet the information requirements can be found on the APHIS website (\u00a7340.4(a)(4)). APHIS is publishing a Draft Regulatory Status Review Guide to provide more detailed information on how to prepare a submission for Regulatory Status Review. This Draft Regulatory Status Review Guide will be available for public review and comment beginning August 25, 2021, and ending October 25, 2021. If you wish to view the document and submit a comment, click on the \"Browse & Comment on Documents\" link. ", "agencyId": "APHIS", "program": "Biotechnology Regulatory Services", "shortTitle": null, "subType2": null, "title": "Draft Guidance for Requesting a Regulatory Status Review under 7 CFR part 340", "generic": null, "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": null, "subType": null, "category": "Genetically Modified Organisms and Products", "field2": null, "effectiveDate": null, "objectId": "0b00006484c78e06"} single_get

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