起草生物材料转让协议:生物库和生物储存库的准备签署模型

S. Cervo, P. De Paoli, Ermes Mestroni, T. Perin, L. Escoffier, V. Canzonieri, A. Steffan
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引用次数: 8

摘要

由于缺乏出版物、指南和国家法规之间的协调,生物库和机构在起草材料转移协议(MTA)时面临着实践和理论问题,MTA是规范生物样品和信息成功交换的基本工具。由于普遍缺乏这方面的知识,研究人员经常不执行mta。因此,开发新的模型以防止研究人员和生物库失去可追溯性和机会、暴露于各种风险以及转移生物材料的延迟是至关重要的。方法通过机构团体和具有多学科专业知识的专业人员的参与,我们为CRO- biobank(国家癌症研究所的生物银行,CRO, Aviano)起草了一份准备签署的MTA,这是一个可以用作即用型协议的标准化模板。研究小组确定了MTA的基本组成部分,包括i)许可、责任和陈述;Ii)托管和分配限制;Iii)材料的适当使用,包括生物安全问题;Iv)保密、不披露和公开;(五)对提供方和接收方的知识产权保护。本文旨在成为一份完整的报告(现有文献中为数不多的作品之一),提供与MTA形成相关的整个过程的描述。生物银行和机构可以考虑采用我们的即签表格作为标准模型。本文讨论了在起草文件期间处理的最重要的问题,从而为面临同样问题的其他机构提出了一种可行的办法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drafting Biological Material Transfer Agreement: A Ready-To-Sign Model for Biobanks and Biorepositories
Purpose Due to the scarcity of publications, guidelines, and harmonization among national regulations, biobanks and institutions face practical and theoretical issues when drafting a material transfer agreement (MTA), the fundamental tool to regulate the successful exchange of biosamples and information. Frequently researchers do not execute MTAs because of a general lack of knowledge about this topic. It is thus critical to develop new models to prevent loss of traceability and opportunities both for researchers and biobanks, their exposure to various risks, and delays in transferring biomaterials. Methods Through the involvement of institutional groups and professionals with multidisciplinary expertise, we have drawn up a ready-to-sign MTA for the CRO-Biobank (the biobank of the National Cancer Institute, CRO, Aviano), a standardized template that can be employed as a ready-to-use model agreement. Results The team identified the essential components to be included in the MTA, which comprise i) permissions, liability and representations; ii) custodianship and distribution limitations; iii) appropriate use of materials, including biosafety concerns; iv) confidentiality, non-disclosure, and publications; v) intellectual property protection for both the provider and recipient. Conclusions This paper aims to be an unabridged report (among the few works in the existing literature) providing a description of the whole process related to the formation of an MTA. Biobanks and institutions may consider adopting our ready-to-sign form as a standard model. The article discusses the most important issues tackled during the drafting of the document, thus proposing an operative approach for other institutions that face the same problems.
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