{"abstract":"The Food and Drug Administration (FDA) is announcing that the proposed collection of information listed below has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995 ( the PRA).","action":"Notice.","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2003/03/07/03-5355.html","cfr_references":[],"citation":"68 FR 11117","comment_url":null,"comments_close_on":"2003-04-07","correction_of":null,"corrections":[],"dates":"Submit written comments on the collection of information by April 7, 2003.","disposition_notes":null,"docket_ids":["Docket No. 02N-0383"],"dockets":[{"supporting_documents":[],"agency_name":"FDA","documents":[{"comment_count":5,"comment_start_date":"2003-03-07","updated_at":"2025-05-13T00:56:16.794-04:00","comment_url":"https://www.regulations.gov/commenton/FDA-2002-N-0101-0001","allow_late_comments":false,"id":"FDA-2002-N-0101-0001","comment_end_date":"2003-04-08","regulations_dot_gov_open_for_comment":false}],"supporting_documents_count":0,"id":"FDA-2002-N-0101","title":"Veterinary Adverse Drug Reaction; Product Defect Report"}],"document_number":"03-5355","effective_on":null,"end_page":11118,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2003/03/07/03-5355.xml","html_url":"https://www.federalregister.gov/documents/2003/03/07/03-5355/agency-information-collection-activities-submission-for-omb-review-comment-request-veterinary","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/03-5355?publication_date=2003-03-07","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2003-03-07/03-5355/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":6,"last_updated":"2026-04-04 16:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2003-03-07/pdf/03-5355.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2003-03-07","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2003/03/07/03-5355.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[],"comments_count":5,"agency_id":"FDA","comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2002-N-0101","supporting_documents_count":0,"docket_id":"FDA-2002-N-0101","document_id":"FDA-2002-N-0101-0001","regulation_id_number":null,"title":"Veterinary Adverse Drug Reaction; Product Defect Report","checked_regulationsdotgov_at":"2025-05-14T07:55:04Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":11117,"subtype":null,"title":"Agency Information Collection Activities; Submission for OMB Review; Comment Request; Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report","toc_doc":"Agency information collection activities; proposals, submissions, and approvals","toc_subject":null,"topics":[],"type":"Notice","volume":68}