临床试验的最新趋势:综述

Rupak K. Swain, Jnyana R. Panda, Rajaram Das, Satyajeet Behera, Sujit K. Patro
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引用次数: 0

摘要

临床研究是一种旨在通过重要阶段检验药物安全性和有效性的研究设计,通常在人类志愿者中进行,以提供有助于人类福祉的安全药物。通常,有效的临床试验研究遵循ICH-GCP政策发布的某些指导方针。这些指导方针和政策旨在保护受试者的利益,并在临床试验中获得有关药物的有价值的信息。许多研究设计是为了获得有关研究的科学信息,因为它是繁琐和昂贵的。
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Recent Trends in Clinical Trials: An Overview
Clinical research is the study design intended to check the safety and efficacy of drugs through the important phases, generally conducted in human volunteers to provide safe medications that contribute to well being of humanity. Generally a effective clinical trial study follows certain guidelines issued by ICH-GCP policies. These guidelines and policies are designed for protecting the interest of subjects and obtaining valuable information about the drug in clinical trial. Many research designs are implemented to obtain scientific information about the research study since it is tedious and expensive.
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