Current practice and perspectives in CRO oversight based on a survey performed among members of the German Association of Research-Based Pharmaceutical Companies (vfa)

Q1 Medicine
M. Hennig, F. Hundt, Susanne Busta, Stefan Mikus, Per-Holger Sanden, Andrea Sörgel, T. Ruppert
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引用次数: 4

Abstract

In recent years, the number and scope of outsourced activities in the pharmaceutical industry have increased heavily. In addition, also the type of outsourcing has changed significantly in that time. This raises the question of whether and how sponsors retain the capability to select and to control the contract research organizations (CROs) involved and what expertise still has to be present in the development department as well as other relevant departments to ensure adequate oversight, also in line with the expectations of regulators and health authorities. In order to answer these questions, a survey was conducted among the German vfa member companies. The survey describes the latest developments and experiences in outsourcing by 18 German vfa member companies. It concentrates on measures how to implement Quality Assurance (QA) when performing outsourced clinical studies. This study shows that the majority of companies apply a full-outsourcing, preferred-provider model of clinical trial services, with the clinical research department playing the major role in this process. A large amount of guiding documents, processes and tools are used to ensure an adequate oversight of the services performed by the CRO(s). Finally the guiding principles for all oversight processes should be transparent communication, a clearly established expectation for quality, a precise definition of accountability and responsibility while avoiding silo mentality, and a comprehensive documentation of the oversight’s evidence. For globally acting and outsourcing sponsors, oversight processes need to be aligned with regards to local and global perspectives. This survey shows that the current implementation of oversight processes in the participating companies covers all relevant areas to ensure highest quality and integrity of the data produced by the outsourced clinical trial.
基于对德国研究型制药公司协会(vfa)成员进行的一项调查,CRO监管的当前实践和观点
近年来,制药行业外包活动的数量和范围大大增加。此外,外包的类型也在那个时候发生了很大的变化。这就提出了一个问题,即资助方是否以及如何保留选择和控制所涉及的合同研究组织(cro)的能力,以及开发部门和其他相关部门仍然需要哪些专门知识来确保充分的监督,也符合监管机构和卫生当局的期望。为了回答这些问题,我们在德国vfa会员公司中进行了一项调查。该调查描述了18家德国vfa成员公司在外包方面的最新发展和经验。它集中于在进行外包临床研究时如何实施质量保证(QA)的措施。本研究表明,大多数企业的临床试验服务采用全外包、首选提供者模式,临床研究部门在这一过程中起着主要作用。我们使用了大量的指导性文件、程序和工具,以确保对投诉专员所提供的服务进行充分的监督。最后,所有监督过程的指导原则应该是透明的沟通、对质量的明确期望、对责任和责任的精确定义,同时避免筒仓思维,以及对监督证据的全面记录。对于全球行动和外包发起人来说,监督过程需要与本地和全球视角保持一致。该调查显示,参与公司目前实施的监督流程涵盖了所有相关领域,以确保外包临床试验产生的数据的最高质量和完整性。
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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来源期刊
GMS German Medical Science
GMS German Medical Science Medicine-Medicine (all)
CiteScore
6.30
自引率
0.00%
发文量
10
审稿时长
11 weeks
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