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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.080 Sterilization and disinfection>11.080.20 Disinfectants and antiseptics>BS EN 1657:2024 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1)
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BS EN 1657:2024 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1)

BS EN 1657:2024

Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1)

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Standard number:BS EN 1657:2024
Pages:52
Released:2024-12-19
ISBN:978 0 539 23188 5
Status:Standard
BS EN 1657:2024 - Chemical Disinfectants and Antiseptics

BS EN 1657:2024 - Chemical Disinfectants and Antiseptics

Introducing the BS EN 1657:2024, a comprehensive standard that sets the benchmark for evaluating the fungicidal or yeasticidal activity of chemical disinfectants and antiseptics specifically used in the veterinary field. This standard is an essential tool for professionals seeking to ensure the highest levels of hygiene and safety in veterinary environments.

Overview

The BS EN 1657:2024 standard provides a detailed quantitative suspension test method, which is crucial for assessing the effectiveness of chemical disinfectants and antiseptics. This standard is part of a series of tests designed to ensure that these products meet stringent requirements for fungicidal and yeasticidal activity, thereby safeguarding animal health and preventing the spread of infections.

Key Features

  • Standard Number: BS EN 1657:2024
  • Pages: 52
  • Release Date: December 19, 2024
  • ISBN: 978 0 539 23188 5
  • Status: Standard

Why Choose BS EN 1657:2024?

This standard is indispensable for manufacturers, laboratories, and veterinary professionals who are involved in the development, testing, and application of chemical disinfectants and antiseptics. By adhering to the guidelines set forth in BS EN 1657:2024, you can ensure that your products are effective against fungi and yeasts, which are common pathogens in veterinary settings.

Comprehensive Testing Methodology

The BS EN 1657:2024 standard outlines a rigorous testing methodology that provides reliable and reproducible results. This ensures that the disinfectants and antiseptics you use or produce are capable of achieving the desired level of microbial control, thereby maintaining a safe and hygienic environment for animals.

Ensuring Veterinary Safety

In the veterinary field, the control of microbial contamination is critical. Fungi and yeasts can pose significant health risks to animals, leading to infections that can be difficult to treat. By following the BS EN 1657:2024 standard, you can be confident that your disinfectants and antiseptics are up to the task of eliminating these pathogens effectively.

Applications

The BS EN 1657:2024 standard is applicable to a wide range of products used in veterinary settings, including:

  • Surface disinfectants
  • Instrument disinfectants
  • Hand sanitizers
  • Antiseptic solutions

These products are essential in maintaining the health and well-being of animals, as well as ensuring the safety of veterinary staff and facilities.

Benefits of Compliance

Compliance with the BS EN 1657:2024 standard offers numerous benefits, including:

  • Enhanced Product Credibility: Demonstrating adherence to a recognized standard enhances the credibility and marketability of your products.
  • Improved Safety: Ensures that your disinfectants and antiseptics are effective, reducing the risk of infections and promoting animal health.
  • Regulatory Compliance: Helps meet regulatory requirements and industry standards, facilitating smoother market entry and acceptance.

Conclusion

The BS EN 1657:2024 standard is an invaluable resource for anyone involved in the veterinary industry. By providing a clear and effective framework for testing the fungicidal and yeasticidal activity of chemical disinfectants and antiseptics, it ensures that these products are both safe and effective. Whether you are a manufacturer, a laboratory technician, or a veterinary professional, adhering to this standard is a crucial step in maintaining the highest standards of hygiene and safety.

Invest in the BS EN 1657:2024 standard today and take a proactive approach to safeguarding animal health and well-being in your veterinary practice or facility.

DESCRIPTION

BS EN 1657:2024


This standard BS EN 1657:2024 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1) is classified in these ICS categories:
  • 71.100.35 Chemicals for industrial and domestic disinfection purposes
  • 11.080.20 Disinfectants and antiseptics
This document specifies a test method and the minimum requirements for fungicidal or yeasticidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water or - in the case of ready-to-use-products - with water. Products can only be tested at a concentration of 80 % or less, as some dilution is always produced by adding the test organisms and interfering substance. This document applies to products that are used in the veterinary area - i.e. in the breeding, husbandry, production, veterinary care facilities, transport and disposal of all animals except when in the food chain following death and entry into processing industry. This document also applies to products used for teat disinfection. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations". NOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2 This method corresponds to a phase 2 step 1 test.