{"abstract":"The Food and Drug Administration (FDA) is issuing an interim final rule to amend certain regulations regarding the screening and testing of donors of human cells, tissues, and cellular and tissue- based products (HCT/Ps), and related labeling. FDA is taking this action in response to comments from affected interested persons regarding the impracticability of complying with certain regulations as they affect particular HCT/Ps.","action":"Interim final rule; opportunity for public comment.","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/2005/05/25/05-10583.html","cfr_references":[{"chapter":null,"citation_url":null,"part":1271,"title":21}],"citation":"70 FR 29949","comment_url":null,"comments_close_on":"2005-08-23","correction_of":null,"corrections":[],"dates":"The interim final rule is effective May 25, 2005. Submit written or electronic comments on the interim final rule by August 23, 2005.","disposition_notes":null,"docket_ids":["Docket No. 1997N-0484T"],"dockets":[],"document_number":"05-10583","effective_on":"2005-05-25","end_page":29952,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2005/05/25/05-10583.xml","html_url":"https://www.federalregister.gov/documents/2005/05/25/05-10583/human-cells-tissues-and-cellular-and-tissue-based-products-donor-screening-and-testing-and-related","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/05-10583?publication_date=2005-05-25","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2005-05-25/05-10583/mods.xml","not_received_for_publication":null,"page_length":4,"page_views":{"count":980,"last_updated":"2026-08-24 00:15:06 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2005-05-25/pdf/05-10583.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2005-05-25","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2005/05/25/05-10583.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"checked_regulationsdotgov_at":"2011-11-12T16:10:34Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":29949,"subtype":null,"title":"Human Cells, Tissues, and Cellular and Tissue-Based Products; Donor Screening and Testing, and Related Labeling","toc_doc":"Human cells, tissues, and cellular and tissue-based products; donor screening and testing, and related labeling","toc_subject":null,"topics":["Communicable diseases","HIV/AIDS","Medical devices","Reporting and recordkeeping requirements"],"type":"Rule","volume":70}