Drafting Biological Material Transfer Agreement: A Ready-To-Sign Model for Biobanks and Biorepositories

Author:

Cervo Silvia12,De Paoli Paolo3,Mestroni Ermes4,Perin Tiziana15,Escoffier Luca6,Canzonieri Vincenzo15,Steffan Agostino12

Affiliation:

1. CRO Biobank, CRO Aviano National Cancer Institute, Aviano (Pordenone) - Italy

2. Clinical Cancer Pathology, CRO Aviano National Cancer Institute, Aviano (Pordenone) - Italy

3. CRO Aviano National Cancer Institute, Aviano (Pordenone) - Italy

4. Technology Transfer Office, CRO Aviano National Cancer Institute, Aviano (Pordenone) - Italy

5. Pathology Division, CRO Aviano National Cancer Institute, Aviano (Pordenone) - Italy

6. Innoventually S.r.l.s., Trieste - Italy

Abstract

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.

Publisher

SAGE Publications

Subject

Cancer Research,Clinical Biochemistry,Oncology,Pathology and Forensic Medicine

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