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Project

Biotechnology - Biobanking - General requirements for biobanking

Abstract

This document specifies general requirements for the competence, impartiality and consistent operation of biobanks including quality control requirements to ensure biological material and data collections of appropriate quality. This document is applicable to all organizations performing biobanking, including biobanking of biological material from multicellular organisms (e.g. human, animal, fungus and plant) and microorganisms for research and development. Biobank users, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others can also use this document in confirming or recognizing the competence of biobanks. This document does not apply to biological material intended for food/feed production, laboratories undertaking analysis for food/feed production, and/or therapeutic use. NOTE 1 International, national or regional regulations or requirements can also apply to specific topics covered in this document. NOTE 2 For entities handling human materials procured and used for diagnostic and treatment purposes ISO 15189 and other clinical standards are intended to apply first and foremost.

Begin

2024-01-04

WI

JT001077

Planned document number

DIN EN ISO 20387 rev

Project number

17600068

Responsible national committee

NA 176-09-02-02 AK - Biobanks/Bioresources  

Responsible european committee

CEN/CLC/JTC 1 - Criteria for conformity assessment bodies  

Responsible international committee

ISO/TC 276/WG 2 - Biobanks and bioresources  

previous edition(s)

Biotechnology - Biobanking - General requirements for biobanking (ISO 20387:2018); German version EN ISO 20387:2020
2020-11

Order from DIN Media

Contact

Dipl.-Ing.

Lena Krieger

Am DIN-Platz, Burggrafenstr. 6
10787 Berlin

Tel.: +49 30 2601-2810
Fax: +49 30 2601-42810

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