Between 3 – 4 million human samples are stored every year in routine medical
care. There are several reasons for biobanking of these samples:
Enhancement of patient disease diagnostics in order to make the best
treatment possible. The means to achieve this goal are:
Control of epidemic infectious diseases by planning and follow up of
infection protection programs and vaccination programs.
Education of medical personel involved in analysis and diagnostics.
Documentation and responsability. If complaints are raised on the
correctness of an analysis, a re-analysis of a stored sample may be performed.
Medical research and quality follow up of medical care. Medical research
makes possible the enhancement of medical care and health. Samples stored during
routine medical care are a valuable source for epidemiological and genetic
studies on the etiology of human diseases.
A smaller number of human samples are collected specifically for research.
Research biobanks may be population based and available for studies of several
kinds of diseases, including common national diseases and cancer diseases. Other
research biobanks have been collected for the study of specific diseases and may
in this respect contain specifically selected tissue samples. Medical research
projects with no primary intention to establish a collection of samples may
store human samples for a limited time during the project.
Research on human samples collected in biobanks must be performed with due
respect to the personal integrity of those people who have provided the samples.
The research must be approved by an ethical committee. The ethical committee
judges if the research is important for medical health and if the risks to
people who have provided the samples, including the personal integrity, are
acceptable. The ethical committee may decide upon information to and specific
approval from people that provided the samples.
All content is © 2003 The National Biobank Program
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