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Gather all necessary information and documents required for the clinical study
02
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Individuals participating in a clinical study
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Clinical study registration and results reporting template, often referred to in shorthand as 'cli nic al st', is a standardized format to submit data regarding clinical trials.
Researchers and sponsors conducting clinical trials that meet certain criteria are required to file clinical study information using the cli nic al st.
To fill out cli nic al st, one must provide comprehensive information about the trial design, eligibility, methodology, as well as results and outcomes of the study.
The primary purpose of cli nic al st is to ensure transparency in clinical research and promote access to results for regulatory bodies, healthcare providers, and the public.
Information such as study title, objectives, study design, participant demographics, outcomes, and results must be reported on cli nic al st.
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