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ISBN 9789351731793 http://www.ayurlog.comISSN 23207329 Vol. 3 Issue: 2nd April June 2015 Analog: National Journal of Research in Ayurveda Science A Web based quarterly online published Open Access
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Obtain necessary training and certification in conducting clinical studies.
02
Develop a detailed protocol outlining the study objectives, procedures, and criteria for participant selection.
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Obtain approval from an institutional review board (IRB) for the study.
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Recruit participants meeting the criteria outlined in the protocol.
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Collect and analyze data according to the study protocol.
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A clinical study is a research study involving human participants that is designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices.
Researchers, sponsors, or institutions conducting the study are required to file a clinical study.
To fill out a clinical study, researchers need to provide detailed information about the study design, objectives, methods, participants, and anticipated outcomes.
The purpose of a clinical study is to gather evidence on the safety and efficacy of new medical interventions to ultimately improve patient care.
Information on the study protocol, informed consent process, participant demographics, study results, and adverse events must be reported on a clinical study.
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