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>BSI Standards >11 HEALTH CARE TECHNOLOGY>11.220 Veterinary medicine>BS EN 18000-2:2026 Animal health diagnostic analyses. Control of in vitro diagnostic reagents Reagents for immunological techniques
immediate downloadReleased: 2026-01-15
BS EN 18000-2:2026 Animal health diagnostic analyses. Control of in vitro diagnostic reagents Reagents for immunological techniques

BS EN 18000-2:2026

Animal health diagnostic analyses. Control of in vitro diagnostic reagents Reagents for immunological techniques

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Standard number:BS EN 18000-2:2026
Pages:18
Released:2026-01-15
ISBN:978 0 539 28221 4
Status:Standard
BS EN 18000-2:2026 - Animal Health Diagnostic Analyses

BS EN 18000-2:2026 - Animal Health Diagnostic Analyses

Introducing the BS EN 18000-2:2026, a comprehensive standard dedicated to the control of in vitro diagnostic reagents specifically designed for immunological techniques in animal health diagnostics. This standard is an essential resource for professionals in the field of veterinary diagnostics, providing a robust framework to ensure the accuracy, reliability, and consistency of diagnostic reagents used in immunological assays.

Key Features of BS EN 18000-2:2026

The BS EN 18000-2:2026 standard is meticulously crafted to address the critical aspects of in vitro diagnostic reagents. Here are some of the key features that make this standard indispensable:

  • Comprehensive Coverage: Spanning across 18 pages, this standard offers an in-depth exploration of the control measures necessary for in vitro diagnostic reagents, ensuring they meet the highest quality standards.
  • Focus on Immunological Techniques: Specifically tailored for reagents used in immunological techniques, this standard provides detailed guidelines to enhance the precision and reliability of diagnostic results.
  • Up-to-Date Information: Released on January 15, 2026, the BS EN 18000-2:2026 incorporates the latest advancements and best practices in the field of animal health diagnostics.
  • Standard Number: BS EN 18000-2:2026, ensuring easy reference and identification within the industry.
  • ISBN: 978 0 539 28221 4, providing a unique identifier for this essential publication.

Why Choose BS EN 18000-2:2026?

In the rapidly evolving field of animal health diagnostics, maintaining the integrity and reliability of diagnostic reagents is paramount. The BS EN 18000-2:2026 standard serves as a critical tool for laboratories, researchers, and manufacturers, offering numerous benefits:

  • Enhanced Diagnostic Accuracy: By adhering to the guidelines set forth in this standard, professionals can ensure that their diagnostic reagents deliver accurate and consistent results, crucial for effective disease management and treatment in animals.
  • Quality Assurance: The standard provides a framework for quality control, helping laboratories maintain high standards in their diagnostic processes and build trust with their clients.
  • Regulatory Compliance: Compliance with BS EN 18000-2:2026 ensures that your laboratory meets the necessary regulatory requirements, facilitating smoother operations and reducing the risk of non-compliance penalties.
  • Industry Recognition: Utilizing a recognized standard like BS EN 18000-2:2026 enhances your laboratory's reputation, demonstrating a commitment to excellence and adherence to industry best practices.

Who Should Use This Standard?

The BS EN 18000-2:2026 standard is designed for a wide range of professionals involved in animal health diagnostics, including:

  • Veterinary Laboratories: Ensuring the accuracy and reliability of diagnostic tests is crucial for veterinary laboratories, making this standard an essential resource.
  • Diagnostic Reagent Manufacturers: Manufacturers can utilize this standard to guide the development and quality control of their products, ensuring they meet industry standards.
  • Research Institutions: Researchers involved in the development of new diagnostic techniques and reagents will find this standard invaluable for maintaining high-quality research outputs.
  • Regulatory Bodies: Regulatory authorities can use this standard as a benchmark for evaluating the quality and compliance of diagnostic reagents in the market.

Conclusion

The BS EN 18000-2:2026 standard is a vital tool for anyone involved in the field of animal health diagnostics. By providing a comprehensive framework for the control of in vitro diagnostic reagents, it ensures that these critical components meet the highest standards of quality and reliability. Whether you are a laboratory professional, a manufacturer, or a researcher, this standard will help you achieve excellence in your diagnostic processes, ultimately contributing to better animal health outcomes.

Embrace the future of animal health diagnostics with the BS EN 18000-2:2026 standard and ensure your practices are aligned with the latest industry standards and best practices.

DESCRIPTION

BS EN 18000-2:2026


This standard BS EN 18000-2:2026 Animal health diagnostic analyses. Control of in vitro diagnostic reagents is classified in these ICS categories:
  • 11.220 Veterinary medicine
Dieses Dokument gilt für die Prüfung und Zulassung von in-vitro-diagnostischen Reagenzien für immunologische Analysen im Bereich der Tiergesundheit mit qualitativer Angabe der Testergebnisse. Dieses Dokument gilt für diagnostische Reagenzien mit Priorität auf Infektionskrankheiten (Bakterien, Viren, Pilze oder Parasiten) oder durch Prionen verursachte Krankheiten und entsprechende Tierarten, für die eine Harmonisierung der Praktiken in diesem Bereich erforderlich ist, d. h. für diejenigen, für die der nationale, regionale oder internationale Regelungsrahmen die Prüfung des Handels mit Tieren und/oder tierischen Erzeugnissen und/oder die Festlegung eines Gesundheitsstatus (Infektionsfreiheit) von Gebieten, Einrichtungen oder Individuen vorsieht. Auch wenn alle von den zuständigen Behörden bezeichneten Reagenzien in den Anwendungsbereich dieses Dokuments fallen, können die Behörden oder andere interessierte Parteien im Bereich der Tiergesundheit sich dazu entschließen, in bestimmten Situationen und Ausnahmefällen, beispielsweise bei neu aufkommenden, exotischen oder seltenen Krankheiten, davon abzuweichen. Dieses Dokument ist nicht auf alle vorhandenen diagnostischen Reagenzien anwendbar, insbesondere nicht auf solche, für die bestimmte in diesem Dokument beschriebene Parameter nicht in Übereinstimmung mit internationalen Anforderungen gültig bewertet werden können, z. B. weil kein spezifisches Referenzverfahren und/oder keine zugänglichen und ordnungsgemäß validierten Referenzmaterialien (RM) zur Verfügung stehen. In diesem Dokument wird nicht der Schritt der Verifizierung eines Reagenzes durch den Anwender behandelt (Annahme eines Analyseverfahrens).