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ISO 7554-3:2026 Surgical instruments — Terms, measuring methods and test methods — Part 3: Test methods

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ISO 41002:2026 Facility management — Development of the facility management organization

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ISO 39004:2026 Road traffic safety — Good practice for service providers using digital platform

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ISO 20070:2025

ISO 20070:2025 Biotechnology — Biobanking — Requirements for primary containers for storing biological materials in biobanks

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This publication was last reviewed and confirmed in 2025.

Biotechnology — Biobanking — Requirements for primary containers for storing biological materials in biobanks

Description

This document specifies requirements for primary containers intended for the storage of biological materials in biobanks. In addition to general requirements, this document also specifies special requirements depending on the storage conditions, the biological material and the intended use, as well as requirements for documentation and quality control. These requirements establish the framework for ensuring that primary containers meet the necessary quality criteria.

This document specifies test criteria and test methods that enable proof of conformity with the requirements.

This document is primarily aimed at manufacturers that produce primary containers for the storage of biological materials. Biobanks, submitters and users of biological material, and organizations that monitor or control the work of biobanks can also use this document.

NOTE            For primary containers intended for biological material for therapeutic use, other requirements can apply.

Edition

1

Published Date

2026-06-19

Status

PUBLISHED

Pages

16

Language Detail Icon

English

Format Secure Icon

Secure PDF

Abstract

This document specifies requirements for primary containers intended for the storage of biological materials in biobanks. In addition to general requirements, this document also specifies special requirements depending on the storage conditions, the biological material and the intended use, as well as requirements for documentation and quality control. These requirements establish the framework for ensuring that primary containers meet the necessary quality criteria.

This document specifies test criteria and test methods that enable proof of conformity with the requirements.

This document is primarily aimed at manufacturers that produce primary containers for the storage of biological materials. Biobanks, submitters and users of biological material, and organizations that monitor or control the work of biobanks can also use this document.

NOTE            For primary containers intended for biological material for therapeutic use, other requirements can apply.

Previous Editions

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