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30 年来的良好实验室规范:行业面临的挑战

Good laboratory practice 30 years on: challenges for industry.

作者信息

Goodwin Mark

机构信息

Preclinical Compliance, Glaxo SmithKline, Park Road, Ware, Hertfordshire SG12 0DP, UK.

出版信息

Ann Ist Super Sanita. 2008;44(4):369-73.

PMID:19351998
Abstract

The principles of good laboratory practice (GLP) have undergone little change since they were established 30 years ago. Conversely, there have been huge advances in science and technology during this time. Test facilities (TF) have been challenged to utilise these advancements and thus enhance the quality of their programmes of non-clinical safety testing. As a consequence, practices are very different today compared with the late 1970's. The scientific advancements have also extended the boundaries of GLP principles and TF must maintain an awareness of the scope of GLP. TF now typically operate on a global basis and strive for harmonised systems, processes and procedures. This is particularly challenging when national monitoring authorities (MA) have different expectations and interpretations of the GLP principles. Other industry challenges that have emerged in recent years include the management of multi-site studies and the independence of the quality assurance (QA) unit.

摘要

自30年前良好实验室规范(GLP)原则确立以来,其变化甚微。相反,在此期间科学技术取得了巨大进步。测试设施(TF)面临着利用这些进步的挑战,从而提高其非临床安全性测试项目的质量。因此,与20世纪70年代末相比,如今的做法大不相同。科学进步也扩展了GLP原则的范围,测试设施必须对GLP的范围保持认识。测试设施现在通常在全球范围内运作,并努力实现系统、流程和程序的统一。当国家监管当局(MA)对GLP原则有不同期望和解释时,这尤其具有挑战性。近年来出现的其他行业挑战包括多地点研究的管理以及质量保证(QA)部门的独立性。

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1
Good laboratory practice 30 years on: challenges for industry.30 年来的良好实验室规范:行业面临的挑战
Ann Ist Super Sanita. 2008;44(4):369-73.
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Differences in the interpretation of the GLP requirements by OECD monitoring authorities: the point of view from the pharmaceutical industry.
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Responsibilities of test facility management and sponsor in a GLP environment.在良好实验室规范(GLP)环境下测试设施管理和申办者的职责。
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