{"database": "openregs", "table": "federal_register", "rows": [["2014-22522", "Medical Use of Byproduct Material-Medical Event Definitions, Training and Experience, and Clarifying Amendments; Correction", "Proposed Rule", "The U.S. Nuclear Regulatory Commission (NRC) published a proposed rule appearing in the Federal Register (FR) on July 21, 2014, to amend the NRC's regulations related to the medical use of byproduct material. The public comment period for the information collection aspects of the proposed rule was to have ended on August 20, 2014. However, the proposed rule inadvertently omitted the one-time implementation costs from the information collection burden estimate. This action sets out the corrected information collection burden estimate in its entirety and allows the public 30 days to comment from the date of publication of this action.", "2014-09-22", 2014, 9, "https://www.federalregister.gov/documents/2014/09/22/2014-22522/medical-use-of-byproduct-material-medical-event-definitions-training-and-experience-and-clarifying", "https://www.govinfo.gov/content/pkg/FR-2014-09-22/pdf/2014-22522.pdf", "Nuclear Regulatory Commission", "383", "The U.S. Nuclear Regulatory Commission (NRC) published a proposed rule appearing in the Federal Register (FR) on July 21, 2014, to amend the NRC's regulations related to the medical use of byproduct material. The public comment period for the...", null]], "columns": ["document_number", "title", "type", "abstract", "publication_date", "pub_year", "pub_month", "html_url", "pdf_url", "agency_names", "agency_ids", "excerpts", "regulation_id_numbers"], "primary_keys": ["document_number"], "primary_key_values": ["2014-22522"], "units": {}, "query_ms": 3.807154018431902, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}