Biobank Lifespan

documents
This 2008 document provides a comprehensive foundation for the guidance of repository activities on the management of human specimen collections.
This document aims to help biomedical researchers undertaking studies and systematic reviews in human genome epidemiology to take sensible decisions about methods right through from study design to final analysis. A HuGENet Systematic Review and Meta-Analysis Working Group handbook (2006).
  This document identifies technical; operational; and ethical, legal, and policy best practices in order to ensure a level of consistency and standardization across biospecimen resources. (2011)
This 2007 document focuses on developing recommendations towards common minimal technical standards in order to stimulate the creation, development and networking of Biological Resource Centres (BRCs) at the international level, and, through their use, enhance and improve cancer research worldwid
This 2007 (updated in 2011) document outlines the operational, technical, ethical, legal, and policy best practices for NCI-supported biospecimen resources. Co-written by NCI, National Institute of Health, and US Department of Health and Human Services-co-written document (2007).
The aim of this paper is to provide information relevant for the establishment, management and governance of biobanks in Australia.
This document presents selected Key Health Organizations/Projects involved in Biobanking.
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This comparison chart summarises the content of a number of websites offering information and tools that are useful for the management and analysis of genomic, transcriptomic and proteomic data. A P3G-prepared document (2009).
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This document compares selected reference guidelines written by well-known organizations. These guidelines cover all biobanking steps, i.e. biological sample collection, labelling, processing, and storage applied to a wide range of sample types. A P3G-prepared document (2008).
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Part II of this document deals with issues related to defining every step of the survey organization, from the target population to the recruitment per se. Part III contains protocols and operational guidelines for individual measurements and biological samples collection.
This Policy Statement considers the issue of return of results in the specific context of population genomics and addresses possible modalities for such return.
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This document identifies core elements from the Sample and Data Access Policies of P³G-member biobanks. This was drafted by the Ethics and Policymaking Core, Centre de recherche en droit public (CRDP), Montreal University (2009).
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  The Medical Research Council (MRC) has developed a framework on the feeddback of health-related findings in research to help researchers identify and consider the relevant issues when designing and implementing a policy on the feedback of health-related findings in research. (2014)
The Framework for Responsible Sharing of Genomic and Health-Related Data  has been developed under the auspices of the Regulatory and Ethics Working Group of the Global Alliance for Genomics and Health, in collaboration with many individuals, organizations and committees around the world.
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The Office for Human Research Protections and the U.S.
FRANÇAIS - Le présent document énumère une série d’éléments à considérer lors de la création de politiques d’accès aux données et échantillons de biobanques.
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In support of the Framework for Responsible Sharing of Genomic and Health-Related Data, P3G-IPAC* prepared 3 consent tools for the Global Alliance for Genomics and Health.
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The international Public Population Project in Genomics (P3G), the European Network for Genetic and Genomic Epidemiology (ENGAGE) and the Centre for Health, Law and Emerging Technologies (HeLEX) have decided to develop data sharing principles specific to the context of collaborative international
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