Get your lab register in the national EQA programme

Chemical Research

Immunoassay PT Scheme

NEQAPP’s Clinical Chemistry proficiency testing schemes ensures accuracy, reliability, and consistency of laboratory results. It allows laboratories to evaluate their performance against standardized benchmarks, identify potential errors, and implement corrective actions. Participation in NEQAPP enhances the credibility of test results and fosters continuous improvement.

Medical labs can make certain patient safety by participating in NEQAPP PT Schemes.

Laboratory results guide up to 70% of clinical decisions. Errors can lead to misdiagnosis, wrong treatment, delayed care, or harm. Maintaining patient safety ensures trust, quality care, and compliance with healthcare standards.

Why choose?

High Quality PT Samples

Lyophilized human serum–based control material, simulating patient samples

Comprehensive Reports

Our reports provide actionable insights into a laboratory's diagnostic performance

Our Strengths

Our proficiency testing schemes are designed according to ISO 17043 standard

Most resourceful EQA programme of the country

  • Our EQA team consists of highly qualified professionals
  • We ensure the homogeneity and stability of PT artefacts
  • We have a secure digital platform

Parameters

  • Alpha fetoprotein
  • Carcinoembryonic antigen (CEA)
  • Cortisol
  • Estradiol
  • Ferritin
  • Follicle Stimulating Hormone (FSH)
  • Luteinizing Hormone (LH)
  • Parathyroid Hormone (PTH)
  • Progesterone
  • Prolactin
  • Prostate Specific Antigen (Total)
  • T3 (Total)
  • T4 (Free)
  • Testosterone
  • Thyroid Stimulating Hormone (TSH)

Description

NEQAPP quality controls are used to check the accuracy and consistency of lab testing for the specific analytes registered with the proficiency testing scheme. NEQAPP EQA controls are lyophilized, human serum-based control used to evaluate the performance of a medical laboratory in the proficiency testing round.

Storage

Keep NEQAPP PT control tightly sealed, refrigerated between 2°C and 8°C.

Preparation

  • Reconstitute: Use a volumetric pipette to add 5.0 mL of distilled or deionized water to the vial.
  • Equilibrate: Replace the stopper and let the vial stand for 15 minutes, swirling it occasionally during this time.
  • Homogenize: Immediately before sampling, gently swirl the vial several times to ensure the solution is uniform throughout.
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