Investigator Responsibilities in Clinical Research
نویسندگان
چکیده
منابع مشابه
Investigator responsibilities for clinical research studies: proper staffing can ensure an investigator is compliant.
The Code of Federal Regulations states that a clinical research investigator is responsible for conducting clinical research in compliance with the signed agreement, investigational plan, and U.S. Food and Drug Administration regulations. In order to meet all the research requirements, the proper research staff is critical. A dedicated, experienced clinical research coordinator is key. The rese...
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Background: It seems we are now experiencing “responsibility problems” among medical trainees (MTs) and some of those recently graduated from medical schools in Iran. Training responsible professionals have always been one of the main concerns of medical educators. Nevertheless, there is a dearth of research in the literature on “responsibility” especially from the medical education point of vi...
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Co-Chairs: Robert M. Califf, MD, FACC, Steven E. Nissen, MD, FACC, FAHA Authors: Anthony N. DeMaria, MD, MACC, FAHA, Erik Magnus Ohman, MD, FACC, Bertram Pitt, MD, FACC, FAHA, James T. Willerson, MD, FACC, FAHA Participants: David W. Bilheimer, MD, Jay N. Cohn, MD, FACC, FAHA, David W. Feigal, JR, MD, MPH, Lindsay Hampson, Beverly H. Lorell, MD, FACC, FAHA, Carl J. Pepine, MD, MACC, FAHA, Richa...
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The aim of this study was to determine whether formal clinical research training is of value in the initiation of a successful career as a clinical investigator. We conducted a retrospective review of the career choices of all 25 fellows who entered the Academic Clinical Research Track at Brigham and Women's Hospital since its inception in 1995 and examined the impact of formal clinical researc...
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ژورنال
عنوان ژورنال: Ochsner Journal
سال: 2020
ISSN: 1524-5012,1524-5012
DOI: 10.31486/toj.19.0085