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ACHIEVINGDIVERSITY, INCLUSION, AND EQUITY IN CLINICAL RESEARCH Toolkit Barbara E. Bearer, MD Sarah A. White, MPH Laura G. Maloney, MPH, MS Hay at R. Ahmed, MS David H. Strauss, MD Luther T. Clark,
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Barbara E. Bierer's research primarily focuses on compliance and regulatory issues related to clinical trials and biomedical research, investigating best practices for promoting ethical standards and protecting participants' rights.
Researchers and institutions conducting clinical trials or biomedical research under her oversight or following her guidelines are typically required to file related documentation.
To fill out Barbara E. Bierer's research documentation, one must provide detailed information about the study design, ethical considerations, participant consent processes, and compliance with regulatory standards.
The purpose of Barbara E. Bierer's research is to enhance the ethical conduct of clinical research, ensure participant protection, and improve the regulatory framework governing biomedical studies.
Key information that must be reported includes study objectives, methodologies, potential risks to participants, informed consent procedures, and data management plans.
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