Checklist to select contract Research Organization for early phase Bioavailability/Bioequivalence Clinical Studies in Healthy Adult Human Volunteers

Sharad Desai, Nilesh Patel
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引用次数: 2

Abstract

Nowadays health agencies of regulated markets are becoming stringent regarding the bio-studies. So clinical/contract research organization (CRO) need to be selected carefully after their detailed assessment. As per requirement of bio-study CRO should be assessed with the study specific checklist of questions before awarding the bio-study. Questions related to various services of study like: Clinic phase, analytical phase, Pharmacokinetic and statistical phase, ethics approval, QA/QC, record handing etc. and related to CRO capabilities are discussed here with their relevance to conclude the abilities of CRO for successful execution of bio-study. Hence, this paper focuses all possible questions which need to be assessed before selection of CRO mainly for Bioavailability/Bioequivalence (BABE) study in healthy adult volunteers. Properly selected CRO will help for smooth execution of study and quality report and subsequently, hassle-free approval of dossier submitted to regulatory agency.
健康成人志愿者早期生物利用度/生物等效性临床研究选择合同研究机构清单
如今,监管市场的卫生机构对生物研究的要求越来越严格。因此,临床/合同研究组织(CRO)需要在对其进行详细评估后慎重选择。根据生物研究的要求,在授予生物研究之前,应使用研究特定问题清单对CRO进行评估。与临床阶段、分析阶段、药代动力学和统计阶段、伦理审批、QA/QC、记录处理等研究的各种服务相关的问题,以及与CRO能力相关的问题,在这里进行讨论,并总结CRO成功执行生物研究的能力。因此,本文主要针对健康成人志愿者的生物利用度/生物等效性(BABE)研究中CRO选择前可能需要评估的所有问题。正确选择CRO将有助于研究和质量报告的顺利执行,随后,提交给监管机构的档案获得无障碍批准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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