{"abstract":"The Nuclear Regulatory Commission (NRC) is amending its regulations to correct or clarify the rule language in several sections in the regulations that govern specific domestic licenses to manufacture or transfer certain items containing byproduct material and medical use of byproduct material. The regulations that govern medical use of byproduct materials were amended in their entirety on April 24, 2002 (67 FR 20249). Subsequently, these regulations were amended again to revise the training and experience requirements for the medical use of byproduct material on March 30, 2005 (70 FR 16336). Through implementation of these revised regulations, the NRC has identified additional changes that need to be made to these regulations. This action is necessary to clarify certain provisions and to make certain conforming changes to the regulations.","action":"Direct final rule.","agencies":[{"raw_name":"NUCLEAR REGULATORY COMMISSION","name":"Nuclear Regulatory Commission","id":383,"url":"https://www.federalregister.gov/agencies/nuclear-regulatory-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/383","parent_id":null,"slug":"nuclear-regulatory-commission"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2007/08/13/07-3976.html","cfr_references":[{"chapter":null,"citation_url":null,"part":32,"title":10},{"chapter":null,"citation_url":null,"part":35,"title":10}],"citation":"72 FR 45147","comment_url":null,"comments_close_on":"2007-09-12","correction_of":null,"corrections":[],"dates":"The final rule is effective on October 29, 2007, unless significant adverse comments are received by September 12, 2007. A significant adverse comment is a comment where the commenter explains why the rule would be inappropriate, including challenges to the rule's underlying premise or approach, or would be ineffective or unacceptable without a change. If the rule is withdrawn due to significant adverse comments, timely notice will be provided in the Federal Register.","disposition_notes":null,"docket_ids":[],"dockets":[],"document_number":"07-3976","effective_on":"2007-10-29","end_page":45151,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2007/08/13/07-3976.xml","html_url":"https://www.federalregister.gov/documents/2007/08/13/07-3976/medical-use-of-byproduct-material-minor-corrections-and-clarifications","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/07-3976?publication_date=2007-08-13","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2007-08-13/07-3976/mods.xml","not_received_for_publication":null,"page_length":5,"page_views":{"count":182,"last_updated":"2026-07-26 10:15:03 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2007-08-13/pdf/07-3976.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"2007-08-13","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2007/08/13/07-3976.txt","regulation_id_number_info":{"3150-AI14":null},"regulation_id_numbers":["3150-AI14"],"regulations_dot_gov_info":{"checked_regulationsdotgov_at":"2011-11-12T22:20:14Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":45147,"subtype":null,"title":"Medical Use of Byproduct Material-Minor Corrections and Clarifications","toc_doc":"Corrections and clarifications","toc_subject":"Byproduct material; medical use:","topics":["Drugs","Health facilities","Health professions","Labeling","Medical devices","Nuclear materials","Occupational safety and health","Radiation protection","Reporting and recordkeeping requirements"],"type":"Rule","volume":72}