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HF 2075 (LSB 5238HV (2) 83)REQUIRING HEALTH BENEFIT COVERAGE FOR CERTAIN CANCER TREATMENT DELIVERED PURSUANT TO APPROVED CANCER CLINICAL TRIALS AND PROVIDING AN APPLICABILITY DATE.BE IT ENACTED BY
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Clinical trials in humans are research studies performed on human participants to evaluate the effects, safety, and efficacy of new medical interventions, treatments, or medications.
Researchers, sponsors, or institutions conducting clinical trials are required to file clinical trials in humans, typically to regulatory authorities such as the FDA or EMA.
To fill out a clinical trial application, researchers must provide detailed information including study design, objectives, participant criteria, intervention methods, ethical considerations, and data management plans.
The purpose of clinical trials in humans is to gather data on the effectiveness and safety of new therapies or medications before they can be approved for general use.
Information reported on clinical trials must include study protocol, informed consent documents, results of the trial, adverse event reporting, and any modifications to the study design.
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