PD ISO/TS 11796:2023
Biological evaluation of medical devices. Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices
| Standard number: | PD ISO/TS 11796:2023 |
| Pages: | 44 |
| Released: | 2023-08-02 |
| ISBN: | 978 0 539 23352 0 |
| Status: | Standard |
PD ISO/TS 11796:2023 Biological Evaluation of Medical Devices
Introducing the PD ISO/TS 11796:2023, a comprehensive guide that sets the standard for the biological evaluation of medical devices. This document is a must-have for any professional in the medical field, particularly those involved in the development, testing, and application of medical devices. It provides a detailed framework for conducting interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices.
Key Features
The PD ISO/TS 11796:2023 is a 44-page document that is packed with valuable information. It is meticulously organized and written in a clear, concise manner to ensure easy comprehension. The standard number, PD ISO/TS 11796:2023, is a testament to its credibility and reliability. It was released on August 2, 2023, ensuring that it contains the most up-to-date information and guidelines.
One of the key features of this document is its focus on the requirements for interlaboratory studies. These studies are crucial in the medical field as they allow for the comparison of results from different laboratories, ensuring consistency and reliability. The PD ISO/TS 11796:2023 provides a detailed guide on how to conduct these studies effectively and accurately.
Another important feature of the PD ISO/TS 11796:2023 is its emphasis on the use of validated in vitro methods to assess the skin sensitization of medical devices. Skin sensitization is a major concern when it comes to medical devices, and this document provides a comprehensive guide on how to assess this using validated in vitro methods.
Why Choose PD ISO/TS 11796:2023?
The PD ISO/TS 11796:2023 is a trusted standard in the medical field. It is backed by the International Organization for Standardization (ISO), a reputable organization known for its high-quality standards. The ISBN number, 978 0 539 23352 0, further attests to its authenticity and credibility.
Choosing the PD ISO/TS 11796:2023 means choosing a document that is comprehensive, reliable, and up-to-date. It is a valuable resource for any professional in the medical field, providing them with the knowledge and guidelines they need to conduct effective and accurate interlaboratory studies and assess the skin sensitization of medical devices using validated in vitro methods.
With the PD ISO/TS 11796:2023, you can ensure that your work is in line with the latest standards and guidelines in the medical field. It is a valuable investment that can greatly enhance the quality of your work and contribute to the advancement of the medical field.
Order Your Copy Today
Don't miss out on this valuable resource. Order your copy of the PD ISO/TS 11796:2023 today and take your work in the medical field to the next level. Remember, knowledge is power, and with the PD ISO/TS 11796:2023, you have the power to make a significant impact in the medical field.
PD ISO/TS 11796:2023
This standard PD ISO/TS 11796:2023 Biological evaluation of medical devices. Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devices is classified in these ICS categories:
- 11.100.20 Biological evaluation of medical devices