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STATE OF CALIFORNIA VICTIM COMPENSATION AND GOVERNMENT CLAIMS BOARD GOVERNMENT CLAIMS PROGRAM REGULATIONS Title 2, 630, 631, 631.5, 632, 632.5, 632.11, 632.5, 632.6, 632.7, 632.8, 632.9, 632.10, 632.11
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GCP reg text 15-day refers to the regulation that requires companies to report specific information about their clinical trials to the appropriate regulatory authorities.
Companies conducting clinical trials are required to file gcp reg text 15-day.
To fill out gcp reg text 15-day, companies need to provide detailed information about their clinical trials, including study protocols, results, adverse events, and more.
The purpose of gcp reg text 15-day is to ensure transparency and accountability in clinical trials, and to help regulatory authorities monitor the safety and efficacy of new drugs.
Information that must be reported on gcp reg text 15-day includes study protocols, results, adverse events, and any other relevant information about the clinical trial.
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