Biobanking has developed at a rapid pace in recent years, initiated by the drive for personalized medicine, the need for high-quality biological resources and associated data for scientific research, and technological advancement of analytical platforms for molecular and genetic research.
This book includes guidelines and recommendations for biobanks not only in high-income countries but also in low- and middle-income countries (LMICs). The recommendations are based on validated and/or evidence-based guidelines.
The book also includes sections on sample sharing, ethical, legal, and social issues (ELSI), and harmonization guidelines important to support collaborative research efforts that make use of biological materials. In particular, the section on open access deals with the principles of sharing and provides recommendations for biobanks in relation to sample and data sharing, which is key to establishing research collaboration. The section on governance provides guidelines on governance structures and standard templates for biobanks for a transparent and effective running of the facilities.
This book also benefits from the experience and knowledge gained by IARC from coordinating the LMICs Biobank and Cohort Building Network (BCNet) and managing an international biobank, which contains diverse collections of specimens and data drawn from studies across the world, including the EPIC (European Prospective Investigation into Cancer and Nutrition) collection.
Table of contents
Section 1. Glossary and definitions
Section 2. Role of biobanks in cancer research
Section 3. Recommendations for biobanks
Section 4. Selected protocols
Annex 1. IARC policy on access to human biological materials
Annex 2. Guidelines for informed consent
Annex 3. Template consent form for biobanking
Annex 4. Template Material/Data Transfer Agreement (MTA/DTA)
Annex 5. Biobank, collection, study, and sample minimum data set and associated standards
Disclosures of interests