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Special Counsel Robert Hur is testifying Tuesday in front of the House Judiciary Committee about his report on President Joe Biden's handling of classified documents.. Hur's report concluded that.


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The Food and Drug Administration (FDA) published the Bioresearch Monitoring Technical Conformance Guide in February 2018. The document provides specifications for clinical data submission by pharmaceutical companies used in planning of FDA Bioresearch Monitoring (BIMO) inspections. Three types of information are required: clinical study level.


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FDA's Bioresearch Monitoring (BIMO) program is a comprehensive program of on-site inspections, data audits, and remote regulatory assessments designed to monitor all aspects of the conduct and.


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Special counsel Robert Hur, who declined to charge President Joe Biden while questioning his mental acuity and memory, testified in a congressional hearing.


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Lin Zhang April 08, 2022 Tag: BIMO , FDA , Webinar Favorites The U.S. Food and Drug Administration (FDA) held a webinar on the Bioresearch Monitoring program (BIMO) last month (2/16/2022). The FDA BIMO program is a comprehensive on-site inspections and data audit program for the clinical research industry.


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Bioresearch Monitoring Information and Operations (BIMO) Technical Conformance Guide (TCG) outlines the FDA's expectations for the submission of clinical trial data as part of electronic submissions (eSub) for new drug applications (NDAs), supplemental NDAs (sNDAs), biologics license applications (BLAs), and supplemental BLAs (sBLAs).


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FY 2020 Clinical Investigator 483 Observation Trends Bioresearch Monitoring (BIMO) Metrics - FY'19 Bioresearch Monitoring (BIMO) Metrics - FY'18 Bioresearch Monitoring (BIMO) Metrics - FY'17.


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Watch live coverage as special counsel Robert Hur testifies at a House Judiciary Committee hearing. Hur led an investigation into President Biden's handling of classified documents after he served.


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FDA's Bioresearch Monitoring (BIMO) program is a comprehensive program of on-site inspections and data audits designed to monitor all aspects of the conduct and reporting of FDA regulated.


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