Abstract

The term "biobanking" is often misapplied to any collection of human biological materials (biospecimens) regardless of requirements related to ethical and legal issues or the standardization of different processes involved in tissue collection. A proper definition of biobanks is large collections of biospecimens linked to relevant personal and health information (health records, family history, lifestyle, genetic information) that are held predominantly for use in health and medical research. In addition, the International Organization for Standardization, in illustrating the requirements for biobanking (ISO 20387:2018), stresses the concept of biobanks being legal entities driving the process of acquisition and storage together with some or all of the activities related to collection, preparation, preservation, testing, analysing and distributing defined biological material as well as related information and data. In this review article, we aim to discuss the basic principles of biobanking, spanning from definitions to classification systems, standardization processes and documents, sustainability and ethical and legal requirements. We also deal with emerging specimens that are currently being generated and shaping the so-called next-generation biobanking, and we provide pragmatic examples of cancer-associated biobanking by discussing the process behind the construction of a biobank and the infrastructures supporting the implementation of biobanking in scientific research.
Original languageEnglish
Pages (from-to)233-246
Number of pages14
JournalVirchows Arch.
Volume479
Issue number2
DOIs
Publication statusPublished - Aug 2021

Keywords

  • Accreditation
  • Biological Specimen Banks/classification
  • Biomedical Research/classification
  • Guidelines as Topic
  • Humans
  • Policy Making
  • Precision Medicine/classification
  • Specimen Handling/classification
  • Stakeholder Participation
  • Terminology as Topic

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