BS EN ISO 23118:2021 - Molecular In Vitro Diagnostic Examinations

Welcome to the future of molecular diagnostics with the BS EN ISO 23118:2021 standard. This comprehensive document is your essential guide to the specifications for pre-examination processes in metabolomics, specifically focusing on urine, venous blood serum, and plasma. Released on June 7, 2021, this standard is a pivotal resource for laboratories and professionals in the field of molecular diagnostics.

Why Choose BS EN ISO 23118:2021?

In the rapidly evolving field of molecular diagnostics, precision and accuracy are paramount. The BS EN ISO 23118:2021 standard provides a robust framework to ensure that pre-examination processes are conducted with the highest level of integrity and reliability. This standard is designed to enhance the quality and consistency of metabolomic analyses, which are critical for accurate diagnostic outcomes.

Key Features of the Standard

• Standard Number: BS EN ISO 23118:2021
• Pages: 28
• Release Date: 2021-06-07
• ISBN: 978 0 539 00463 2
• Status: Standard

This standard is meticulously crafted to address the nuances of pre-examination processes in metabolomics. It provides detailed specifications that are crucial for laboratories aiming to maintain high standards of practice in molecular diagnostics.

Comprehensive Coverage

The BS EN ISO 23118:2021 standard covers a wide range of topics essential for the pre-examination phase of metabolomic testing. This includes guidelines for sample collection, handling, and processing, ensuring that every step is optimized for accuracy and reliability. By adhering to these guidelines, laboratories can minimize pre-analytical variability, which is a common source of error in diagnostic testing.

Applications in Metabolomics

Metabolomics is a powerful tool in the field of molecular diagnostics, providing insights into the metabolic state of an organism. The BS EN ISO 23118:2021 standard is specifically tailored to support metabolomic analyses in urine, venous blood serum, and plasma. These biological matrices are commonly used in clinical diagnostics, and this standard ensures that the pre-examination processes are aligned with best practices.

Enhancing Diagnostic Accuracy

Accurate diagnostic results are the cornerstone of effective patient care. The BS EN ISO 23118:2021 standard plays a crucial role in enhancing the accuracy of metabolomic analyses by providing clear and concise guidelines for pre-examination processes. By following these guidelines, laboratories can ensure that their diagnostic results are both reliable and reproducible.

Who Should Use This Standard?

This standard is an invaluable resource for a wide range of professionals in the field of molecular diagnostics, including:

• Clinical laboratory scientists
• Biochemists
• Pathologists
• Research scientists
• Quality assurance professionals

Whether you are involved in routine diagnostic testing or cutting-edge research, the BS EN ISO 23118:2021 standard provides the guidance you need to ensure the highest quality of pre-examination processes.

Invest in Quality and Reliability

In the competitive field of molecular diagnostics, investing in quality and reliability is essential. The BS EN ISO 23118:2021 standard is your assurance of excellence in pre-examination processes. By implementing this standard, you can enhance the credibility of your laboratory and ensure that your diagnostic results are trusted by healthcare professionals and patients alike.

Conclusion

The BS EN ISO 23118:2021 standard is more than just a document; it is a commitment to excellence in molecular diagnostics. With its comprehensive guidelines and specifications, this standard is an indispensable tool for laboratories striving to achieve the highest standards of practice in metabolomics. Embrace the future of diagnostics with confidence by integrating the BS EN ISO 23118:2021 standard into your laboratory's processes.

BS EN ISO 23118:2021

This standard BS EN ISO 23118:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma is classified in these ICS categories:

• 11.100.10 In vitro diagnostic test systems

This document specifies requirements and gives recommendations for the handling, documentation and processing of urine, venous blood plasma and serum intended for metabolomics analysis in the pre-examination processes. This document is applicable to metabolomics examinations and can be used by biomedical laboratories, customers of laboratories, in vitro diagnostics developers and manufacturers, institutions and companies performing biomedical research, biobanks, and regulatory authorities.