Haematology PT Scheme
Proficiency testing in Histopathology scheme is based on sample review.
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?
Haematology PT controls provide objective benchmarking and proficiency assessment
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
- Hematocrit (HCT)
- Hemoglobin (Total)
- Mean Corpuscular Hemoglobin (MCH)
- Mean Corpuscular Hemoglobin Concentration (MCHC)
- Mean Corpuscular Volume (MCV)
- Platelets (PLT)
- Red Blood Cells (RBC)
- White Blood Cells (WBC)
Description
For ease of use, Haematology PT controls are provided in a ready-to-use liquid format
Storage
Keep NEQAPP PT control tightly sealed, refrigerated between 2°C and 8°C.
Preparation
- If refrigerated, allow the PT vial to warm to room temperature (15 to 30°C) for 15 minutes before mixing. To mix, hold a tube horizontally between the palms of your hands. Do not pre-mix on a mechanical mixer. Roll the tube back and forth for 20 to 30 seconds; occasionally invert the tube. Mix vigorously, but do not shake. Continue the process until the red cells are completely suspended. Gently invert the tube 8 to 10 times immediately before sampling.