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Independent clinical studies are of key importance for improving the effectiveness, safety and cost/benefit balance, such as the long-term risks and rare adverse reactions to treatments, comparing the available treatment options, evaluating the hoped-for improvements in quality of life or in follow-up of procedures and rehabilitation strategies.
Center for Biologics Evaluation and Research; Center for Global Infectious Disease Research; Center for the Evaluation of Risks to Human Reproduction; Center for the Study of Traumatic Encephalopathy; Centers for Disease Control and Prevention; Centers of Biomedical Research Excellence; Chan Zuckerberg Biohub; Collaborative Study on the ...
This is a list of United States federal agencies that are primarily devoted to research and development, including their notable subdivisions. These agencies are responsible for carrying out the science policy of the United States .
Clinical trials in the US are registered on clinicaltrials.gov. Clinicaltrials.gov is the largest clinical trials registry. Clinical trials conducted in the United States are required to be registered in the registry. Its registrations represent about 75% of what is available through the WHO portal (ICTRP).
In clinical research a research site conducts all or part of a clinical trial. For clinical trials which recruit research participants in multiple locations, often the research will have a headquarters then multiple regional research sites to conduct the research in that region. In a network of research sites where all are recruiting study ...
An independent safety officer (ISO) is a clinician or researcher who is independent of the clinical study team and helps to monitor a clinical trial for research participant (patient) safety, adverse events, trial progress, and data quality. An ISO has relevant experience with clinical trials as well as with the patient population and ...
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