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NATIONAL WORKSHOP ON STUDY DESIGNS IN CLINICAL TRIALS February 34, 2017, Organized by Department of Clinical Pharmacology & Department of Pharmacology SRM Medical College Hospital & Research Center

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What is study designs in clinical?

Study designs in clinical refer to the plan or blueprint that outlines the objectives, methodology, and execution of a clinical study.

Who is required to file study designs in clinical?

Researchers conducting clinical studies are required to file study designs in clinical.

How to fill out study designs in clinical?

To fill out study designs in clinical, researchers must include details on research objectives, study population, methodology, data collection methods, and statistical analysis plan.

What is the purpose of study designs in clinical?

The purpose of study designs in clinical is to ensure that clinical studies are conducted in a structured and ethical manner to produce reliable results.

What information must be reported on study designs in clinical?

Information such as research objectives, study population characteristics, study procedures, data collection methods, statistical analysis plan, and ethical considerations must be reported on study designs in clinical.

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