A moment of TRUTH is near at hand.One of the things I will be...

A moment of TRUTH is near at hand.
One of the things I will be looking for is the news around KRINKO.The Commission for Hospital Hygiene and Infection Prevention (KRINKO).
It is based in KOCH institute. It plays a vital role in developing national recommendations for preventing healthcare-associated infections. These guidelines are applicable not only to hospitals but also to other healthcare facilities
Mr. K was expecting new guidelines and was expecting that ultrasound procedures not only be AUOTOMATED but to be VALIDATED as well.
I expect further developments...............German practices are usually gamechanging

Note.................TROPHON EPR should read Trophon 2
CHATGPT

1. Automated vs. Validated Disinfection:

   • Automated processes involve using machines or devices to perform disinfection tasks. These can be efficient and consistent.
   • However, validation ensures that the process is effective, reliable, and meets specific standards. It involves verifying that the disinfection method achieves the desired outcome (e.g., pathogen elimination) consistently.

2. Validation Steps:

   • Testing: Validation begins with testing the disinfection process using standardized methods. For example, a high-level disinfectant’s efficacy against specific microorganisms is assessed.
   • Parameters: Parameters such as exposure time, concentration, and temperature are defined.
   • Monitoring: Regular monitoring ensures ongoing compliance with validated parameters.
   • Documentation: Detailed records are maintained to demonstrate validation.

3. Challenges:

   • Device Variability: Ultrasound probes vary in design, material, and surface characteristics. Validating a process across different probe types is essential.
   • Real-world Conditions: Validation should consider real-world conditions (e.g., probe handling, user variability).
   • New Technologies: As new disinfection technologies emerge, validation becomes critical.

4. Nanosonics’ Trophon® EPR:

   • This system uses sonicated hydrogen peroxide mist for HLD of ultrasound probes.
   • It has undergone rigorous validation to ensure consistent and effective disinfection.
   • Trophon® EPR’s automated process is complemented by robust validation.

     CertainlyAuditPRO is a Safety and Compliance Inspection Platform used by companies to enhance safety efficiency and demonstrate regulatory compliance¹. While it primarily focuses on safety and compliance, it doesn’t directly validate disinfection processes. However, here are some features of AuditPRO:

     1. Workflow Approval:

        • Collaborate on submissions with multiple users.
        • Pass submissions for approval before they’re submitted to the AuditPro Portal².

     2. Signature Capture:

        • Electronically sign audit reports for added efficiency and legal validity³.

     Remember, for specific validation of disinfection processes like Nanosonics’ trophon® EPR,