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This document provides guidelines for the National External Quality Assessment Scheme for testing sexually transmitted infections (STIs) and transfusion-transmissible infections (TTIs) to ensure quality
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How to fill out GUIDELINES FOR NATIONAL EXTERNAL QUALITY ASSESSMENT SCHEME-STI/TTI SEROLOGY

01
Read the guidelines thoroughly to understand the purpose of the National External Quality Assessment Scheme.
02
Gather all required documentation and materials related to STI/TTI serology testing.
03
Follow the specified format to document your laboratory's quality control processes.
04
Populate the assessment form with accurate and up-to-date information regarding serology testing methods used.
05
Include clarity on personnel qualifications and training relevant to STI/TTI serology.
06
Validate the performance of serology tests used and include results from prior assessments.
07
Submit the completed assessment form by the designated deadline.

Who needs GUIDELINES FOR NATIONAL EXTERNAL QUALITY ASSESSMENT SCHEME-STI/TTI SEROLOGY?

01
Laboratories conducting STI/TTI serology testing.
02
Public health officials overseeing quality assurance in healthcare.
03
Healthcare professionals involved in diagnosing and managing sexually transmitted infections.
04
Regulatory bodies monitoring compliance with health standards.
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The GUIDELINES FOR NATIONAL EXTERNAL QUALITY ASSESSMENT SCHEME-STI/TTI SEROLOGY establishes a standardized framework for assessing the quality of serological testing methods for sexually transmitted infections (STIs) and transfusion-transmissible infections (TTIs) across healthcare facilities.
Healthcare laboratories and facilities that perform serological tests for STIs and TTIs are required to participate in and file under the GUIDELINES FOR NATIONAL EXTERNAL QUALITY ASSESSMENT SCHEME-STI/TTI SEROLOGY.
To fill out the guidelines, laboratories must provide detailed information about their testing processes, results, and quality control measures as specified in the assessment forms provided by the overseeing health authority.
The purpose of these guidelines is to ensure that serological tests for STIs and TTIs are accurate and reliable, improving overall public health outcomes by standardizing testing procedures and quality assessments across all participating laboratories.
Laboratories must report information such as test methodologies, results of proficiency testing, internal quality control data, and any discrepancies or corrective actions taken in response to quality assessment findings.
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