Troponin T Quality Control

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Troponin T Quality Control

Therapeutic Drug Quality Control

Intended for use with the Roche system, this control is manufactured using only the highest quality material and offers an unrivalled 7-day thawed stability at +2ºC to +8ºC.

Features & Benefits

  • Lyophilised for enhanced stability
  • 100% human serum
  • Ultra low levels of Troponin T
  • Stable to expiry date at -(18-24)ºC storage
  • Reconstituted stability of 7 days at 2°C – 8°C
DescriptionSizeAnalytesCat No 
Troponin T Control6 x 3 ml1CQ10450

Analytes

  • Heart Type Fatty Acid Binding Protein

Ethanol Calibrator/Control Set

Therapeutic Drug Quality Control

Dedicated calibrator and control set designed for the calibration and quality control of the Randox Ethanol assay.

Features & Benefits

  • Liquid ready-to-use
  • Human urine
  • Stable to expiry date when capped and stored at 2oC – 8oC
  • Open vial stability of 28 days at 2oC – 8oC
DescriptionSizeAnalytesCat No 
Ethanol Calibrator/Control Set4 x 10ml1DA2703

Analytes

Ethanol


sTfR Quality Control

Therapeutic Drug Quality Control

Providing a true third party solution for the measurement of Soluble Transferrin Receptor (sTfR), the Acusera sTfR Control  will deliver an unbiased, independent assessment of analytical performance.

Designed for used with sTfR assays, this handy single analyte control saves money on wasted material.

Features & Benefits

  • Lyophilised control
  • Human based material
  • Assayed target values available
  • Stable to expiry date at 2°C to 8°C
  • Reconstituted stability of 30 days at 2°C to 8°C
DescriptionSizeAnalytesCat No 
sTfR Control (Bi-level)3 x 2 x 1 ml1TF10162
sTfR Calibrator6 x 1 ml1TF10161

Analytes

  • Soluble Transferrin Receptor (sTfR)

Related Products


Metabolic Syndrome Array II Quality Control

Therapeutic Drug Quality Control

A multi-analyte quality control with target values and ranges provided for 3 parameters associated with metabolic syndrome.

Features & Benefits

  • Lyophilised for enhanced stability
  • 100% human material
  • Stable to expiry date at 2oC – 8oC
  • Reconstituted stability of 72 hours at 2oC – 8oC and 7 days at -20°C
  • Assayed values available for Randox Biochip systems
DescriptionSizeAnalytesCat No 
Metabolic Syndrome Array II Control3 x 3 x 1ml3EV3761
Metabolic Syndrome Array II Calibrator9 x 1 ml3EV3760

Analytes

  • Adiponectin
  • CRP
  • Cystatin C

Liquid HbA1c Quality Control

Therapeutic Drug Quality Control

Conveniently supplied liquid ready-to-use the Liquid HbA1c control is ideally suited to both clinical laboratories and POCT helping to significantly reduce preparation time. With a stability of 30 days waste and costs are also kept to a minimum.

Features & Benefits

  • Liquid ready-to-use
  • Human based whole blood
  • Assayed target values
  • Convenient bi-level pack covering clinically relevant decision levels
  • Stable to expiry date at  2°C – 8°C
  • Open vial stability of 30 days at  2°C – 8°C

DescriptionSizeAnalytesCat No 
Liquid HbA1c Control2 x 2 x 0.5 ml1HA10155
Liquid HbA1c Control Level 16 x 1 ml1HA10224
Liquid HbA1c Control Level 26 x 1 ml1HA10225

Analytes

HbA1c (Haemoglobin A1c)


How frequently should you run EQA?

There is much debate among clinical laboratories when discussing this common question. With some schemes offering testing as little as 2 times per year, it raises the question, is this really enough?

How frequently an EQA scheme is run will often be dependent on several aspects. Factors such as the diagnostic error rate, number of tests undertaken, experience and turnover of technical staff, and the known stability/instability of the analyte in question should be considered and will all contribute to determine the desired frequency of EQA.

Each EQA programme will vary, where one area, for instance Chemistry, may require bi-weekly testing, another, such as Serology, may only need to be tested every 3 months. Although there is variation between schemes, the benefits of testing more frequently unquestionably outweighs the costs of not testing frequently enough.

Issues with infrequent testing?

If your EQA provider offers infrequent testing, there is likely to be a lengthy period of uncertainty where errors could be happening in the laboratory and consequently incorrect results being released. The outcome of this could be damaging to both patients and laboratories, with credibility and trust in results likely to come under scrutiny. For these reasons, having an infrequent EQA scheme could cause harm to your laboratory and reduce confidence in your test results.

Why should you use a frequent EQA scheme?

To ensure the previously mentioned errors do not occur, laboratories should participate in frequent EQA schemes to guarantee that if incorrect test results do arise, then they will be detected and rectified immediately.

As preventative/corrective actions can be taken sooner through frequent EQA schemes, you will have increased confidence in your test systems performance and may reduce the need for expensive retests. Being able to pinpoint when an error occurred will be much simpler if you are only looking back a matter of weeks or a couple months, as opposed to if you are looking back over a longer period such as 4 to 6 months.

The ability to implement corrective actions sooner and with less disruptions to the lab will help lead to both time and cost savings in the future.

What can Randox Quality Control offer?

Randox International Quality Assessment Scheme (RIQAS), offers bi-weekly, monthly and quarterly reporting options* designed to assist with the early identification of laboratory errors. Not only will RIQAS provide you with extra confidence in test system accuracy, but with 32 flexible programmes you could also make significant cost and time savings through consolidation.

With more than 40,000 participants in 124 countries, RIQAS is the largest international EQA scheme on the market and offers laboratories around the world assurances that the results they are releasing are accurate and reliable. Our many features include; the ability to register up to 5 instruments per programme at no extra cost, easy to read reports, internationally accredited programmes and rapid report turnaround. Why don’t you contact us today and find out how we can support you in maintaining quality control in your laboratory?

*Programme Specific


Liquid CSF Quality Control

Therapeutic Drug Quality Control

Providing a true third party solution for the measurement of Cerebrospinal Fluid (CSF), the Acusera Liquid CSF Control is designed to deliver an unbiased, independent assessment of analytical performance for 14 analytes, helping to ensure the results clinical laboratories release are accurate and reliable.

With an extended open vial stability of 30 days at 2oC – 8oC, the Acusera Liquid CSF Control will reduce waste, while remaining easy and convenient to use.

Features & Benefits

  • Liquid ready-to-use samples requiring no preparation
  • Human based material
  • True third party control providing unbiased performance assessment
  • Assayed target values available
  • Shelf life of 2 years from the date of manufacture
  • Open vial stability of 30 days for all analytes when stored at 2oC to 8oC
DescriptionSizeAnalytesCat No 
Liquid CSF Control Level 110 x 3ml14CF10138
Liquid CSF Control Level 210 x 3ml14CF10139

Analytes

  • Albumin (electrophoresis)
  • Alpha – 1- globulin (electrophoresis)
  • Alpha – 2- globulin (electrophoresis)
  • Beta- globulin (electrophoresis)
  • Chloride
  • Gamma – globulin (electrophoresis)
  • Glucose
  • hsIgA*
  • hsIgG
  • hsIgM*
  • Lactate
  • Microalbumin
  • Protein (Total)
  • Sodium

*No claims are made regarding values and stability.


PTH Quality Control

Therapeutic Drug Quality Control

Providing a true third party solution for the measurement of Intact PTH, the new Acusera PTH Control will deliver an unbiased,
independent assessment of analytical performance with any instrument or method.

This notoriously unstable marker, present in a number of immunoassay controls, is now available in a liquid frozen format with an impressive 30 day open vial stability, reducing waste while remaining easy-to-use.

Features & Benefits

  • Liquid for ease-of-use
  • 100% human serum
  • Assayed target values available for many immunoassay platforms
  • Stable to expiry date at -20°C to 70°C
  • Open vial stability of 30 days at 2°C to 8°C
DescriptionSizeAnalytesCat No 
PTH Control Level 13 x 3 ml1PTH10110
PTH Control Level 23 x 3 ml1PTH10111
PTH Control Level 33 x 3 ml1PTH10112

Analytes

  • Intact PTH (Parathyroid Hormone)

Related Products


Adiponectin Quality Control

Therapeutic Drug Quality Control

Dedicated Adiponectin control designed for use in routine monitoring of the Randox Adiponectin assay.

Features & Benefits

  • Liquid ready-to-use
  • Human based serum
  • Stable to expiry date at 2°C – 8°C
  • Once opened stable to expiry date at 2°C – 8°C
DescriptionSizeAnalytesCat No 
Adiponectin Control Level 23 x 1ml1AO2815
Adiponectin Control Level 33 x 1ml1AO2816

Analyte

  • Adiponectin

Evidence Immunoassay Control

Therapeutic Drug Quality Control

Multi-analyte immunoassay control designed for use in the routine monitoring of the Randox Fertility, Thyroid and Tumour Marker Arrays.

Features & Benefits

  • Lyophilised for enhanced stability
  • Assayed values available for Randox Biochip systems
  • 100% human serum
  • Stable to expiry date at 2oC – 8oC
  • Reconstituted stability of 7 days at 2oC – 8oC or 4 weeks at -20oC
DescriptionSizeAnalytesCat No 
Evidence Immunoassay Control4 x 3 x 5ml14EV3570

Analytes

  • CEA
  • Estradiol
  • FSH
  • Free T4
  • Free T3
  • Leutinising Hormone
  • Prolactin
  • Progesterone
  • PSA (Total)
  • PSA (Free)
  • Testosterone
  • Total T4
  • Total T3
  • TSH

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