BS ISO 21899:2020 - Biotechnology Biobanking Standard

Welcome to the future of biobanking with the BS ISO 21899:2020 standard. This comprehensive document is a must-have for any biobank aiming to ensure the highest quality and reliability in the processing of biological materials. Released on June 25, 2020, this standard is a pivotal resource for professionals in the biotechnology and biobanking sectors.

Overview

The BS ISO 21899:2020 standard provides a detailed framework for the validation and verification of processing methods for biological materials in biobanks. With a total of 32 pages, this document is meticulously crafted to guide biobanks in maintaining the integrity and quality of their biological samples. The standard is recognized globally and is essential for ensuring compliance with international biobanking practices.

Key Features

• Standard Number: BS ISO 21899:2020
• Pages: 32
• Release Date: June 25, 2020
• ISBN: 978 0 580 51058 8
• Status: Standard

Why Choose BS ISO 21899:2020?

Biobanking is a critical component of modern biotechnology, providing the foundation for research and development in various fields such as medicine, genetics, and pharmaceuticals. The BS ISO 21899:2020 standard is designed to help biobanks achieve excellence in their operations by offering a robust set of guidelines for the validation and verification of processing methods. Here are some reasons why this standard is indispensable:

1. Ensures Quality and Consistency

By adhering to the guidelines set forth in the BS ISO 21899:2020 standard, biobanks can ensure that their processing methods are consistent and of high quality. This consistency is crucial for maintaining the integrity of biological samples, which in turn supports reliable research outcomes.

2. Facilitates Compliance

Compliance with international standards is essential for biobanks that operate on a global scale. The BS ISO 21899:2020 standard provides a clear framework for compliance, helping biobanks meet regulatory requirements and avoid potential legal issues.

3. Enhances Credibility

Biobanks that implement the BS ISO 21899:2020 standard demonstrate their commitment to quality and excellence. This enhances their credibility and reputation in the biotechnology community, attracting more partnerships and collaborations.

4. Supports Innovation

With a solid foundation in place, biobanks can focus on innovation and development. The BS ISO 21899:2020 standard provides the necessary guidelines to ensure that new processing methods are validated and verified, paving the way for groundbreaking research and discoveries.

Who Should Use This Standard?

The BS ISO 21899:2020 standard is ideal for a wide range of professionals and organizations involved in biobanking and biotechnology, including:

• Biobank Managers and Operators
• Quality Assurance Professionals
• Regulatory Compliance Officers
• Research Scientists and Technicians
• Biotechnology Companies

Conclusion

In the rapidly evolving field of biotechnology, staying ahead of the curve is essential. The BS ISO 21899:2020 standard is an invaluable resource that provides the guidance and assurance needed to excel in biobanking. By implementing this standard, biobanks can ensure the highest quality and reliability in their operations, ultimately contributing to the advancement of science and technology.

Invest in the future of your biobank with the BS ISO 21899:2020 standard and join the ranks of leading institutions that prioritize quality, compliance, and innovation.

BS ISO 21899:2020

This standard BS ISO 21899:2020 Biotechnology. Biobanking. General requirements for the validation and verification of processing methods for biological material in biobanks is classified in these ICS categories:

• 07.080 Biology. Botany. Zoology

This document specifies the validation and verification requirements applicable to a biobank to be able to demonstrate that it operates its processing of biological materials with validated and/or verified methods that are fit for purpose.

This document is intended for use in the implementation and validation of processing methods for biological materials.

This document covers method validation and verification for the production of all biological materials. This document does not apply to biological material intended for food/feed production, laboratories undertaking food/feed analysis, and/or therapeutic use.

Reference material production is not covered in this document. For the production requirements for reference materials, see ISO 17034.