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DIN EN ISO 20387:2025-11

Biotechnology - Biobanking - General requirements for biobanks (ISO/DIS 20387:2025); German and English version prEN ISO 20387:2025 / Note: Date of issue 2025-10-24*Intended as replacement for DIN EN ISO 20387 (2020-11), DIN EN ISO 20387/A11 (2024-09).

Fecha edición: 2025-11-01
En Vigor
Idiomas disponibles: Alemán, Inglés
Resumen: This document specifies general requirements for the competence, impartiality and consistent operation of biobanks including quality control requirements to ensure that collections of biological material and associated data are of appropriate quality. This document is applicable to all organizations performing biobanking. This can include biobanking of biological material: a) from multicellular organisms (e. g. human, animal, fungus and plant); b) from microorganisms; c) derived from sources such as environmental samples (e. g. soil, sediment, water, air). 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 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.

Keywords: Biochemicals|Biological|Biological characteristics|Biotechnology|Competence|Data acquisition|Data bases|Data collection|Data exchange|Definitions|Environmental condition|Information interchange|Management|Materials|Preservation|Quality|Quality control|Research|Resources|Sample handling systems|Samples|Sequence of operations|Specification (approval)|Storage|Traceability|Transport
ICS: 07.080 - Biología. Botánica. Zoología
CTN:

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