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QuikRead go wrCRP

QuikRead go wrCRP is a fast and an easy to use test for quantitative determination of C-reactive protein (CRP) values in whole blood, serum and plasma with the QuikRead go instrument. The test gives wide range CRP results within minutes and eases the everyday work in various healthcare settings.


Fast measurement of C-reactive protein (CRP) can be critical in the management of a patient with symptoms of an infection. The easy-to-use QuikRead go wrCRP test can be performed near the patient and the CRP result is immediately available.

A wide range CRP test allows the extension of CRP values from conventional use to testing e.g neonatal sepsis(1) as well as to predict disease severity in COPD(2) and aid in cardiovascular risk assessment(3). Room temperature storage for unopened kit and small sample volume ease the everyday work of the healthcare professionals.

QuikRead go wrCRP is an efficient tool for point-of-care settings to guide the treatment decisions of healthcare professionals.

QuikRead go wrCRP provides you with

Kit storage at room temperature up to 25°C

  • Easy to store in the healthcare unit
  • Enables immediate use, no need to warm up reagents

Wide measuring range

  • Offers wide CRP result from whole blood samples from 0.5 up to 200 mg/l and plasma/serum samples from 0.5 up to 120 mg/l
  • Enables using CRP in wide range of indications

Small sample volume 10 µl

  • Sample collection is easy
  • Improved convenience for the patient

Fast point-of-care CRP test

  • Measurement time only 2 minutes

Easy to use

  • Fully automatic testing procedure


  • QuikRead go instrument is connectable to most HIS and LIS systems

Test results should never be used alone, without a complete clinical evaluation.

QuikRead go wrCRP is not registered in the USA. 



  1. Hengst JM: The role of C-reactive protein in the evaluation and management of infants with suspected sepsis. Adv Neonatal Care 2003; 3:3–13.
  2. Mendy A, Forno E, Niyonsenga T, Gasana J. Clin Respir J. 2017. Blood biomarkers as predictors of long-term mortality in COPD. https://doi.org/10.1111/crj.12752
  3. Kaptoge S, Di Angelantonio E, Lowe G, Pepys MB, Thompson SG, Collins R, Danesh J. C-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant meta-analysis. Emerging Risk Factors Collaboration. 2010 Lancet 375(9709):132-40.


Technical data

Products available
Use For in vitro diagnostic use


Sample type Whole blood, serum, plasma
Instrument information

QuikRead go Instrument

Time to result 2 minutes
Reading of the result Instrument read
Storage 2 - 25 ºC
Additionally needed
  • QuikRead go Instrument 133893
  • Capillaries 147851, supplied with product 146521
  • Plungers 67966, supplied with product 146521
  • QuikRead go wrCRP Control 153038
  • QuikRead go wrCRP Control High 1ml 153039
  • Ultrasensitive CRP Control 1ml 68257
Registration Not registered in the USA
Registered trademark QuikRead go is a registered trademark of Orion Diagnostica Oy.

Related products

Regular use of QuikRead CRP Controls is recommended.

The Controls available are:

  • Ultrasensitive CRP Control, with a concentration of approx. 2-3 mg/l 
  • QuikRead go wrCRP Control, with a concentration of approx. 30 mg/l
  • QuikRead go wrCRP Control High, with a concentration of approx. 80 mg/l


Specific features of CRP (C-reactive protein)

  • normally present in very low concentrations in the blood of healthy people; 99% have levels of <10 mg/l 1 and 90 % have levels < 3 mg/l2.
  • after birth concentrations are very low (0,1 mg/l) and there is a physiological rise during the first days of life (to approx. 2 mg/l)3
  • uncomplicated viral infections mostly induce (with some exceptions) a very modest elevation or none at all1
  • in bacterial infections, concentrations increase markedly1
  • elevated concentrations can be detected within 6 - 12 h after onset of an inflammatory stimulus, reaching maximum within 24 - 48 h4, 5
  • rise in concentrations corresponds to severity of infection1
  • concentrations fall rapidly when the patient responds to antibiotic treatment1
  • normalisation of the concentration may indicate that the duration of the treatment has been sufficient and the treatment can be discontinued1, 6, 7
  • in a big part of septic neonates the concentrations are below 6 mg/l 8, 9, 10



  1. Pepys MB. The acute phase response and C-reactive protein. In: Warrell DA, Cox TM, Firth JD, Benz EJ, eds. Oxford Textbook of Medicine, 4th ed. Oxford University Press, 2003. Vol 2, p.150 - 156.
  2. Shine, B., de Beer, FC., Pepys, MB. Solid phase radioimmunoassays for C-reactive protein. Clin Chim Acta, 1981,117: 13 - 23.
  3. Chiesa, C., Natale, F., Pascone, R., Osborn, JF., Pacifico, L., Bonci, E., De Curtis, M. C reactive protein and procalcitonin: Reference intervals for preterm and term newborns during the early neonatal period. Clinica Chimica Acta, 2011, 412: 1053 - 1059.
  4. Bjerrum L. C-reactive protein measurement in general practice may lead to lower antibiotic prescribing for sinusitis. Br J Gen Pract 2004; 54: 659 - 662.
  5. Pepys MB. C-reactive protein fifty years on. Lancet 1981; 1: 653 - 657.
  6. Philip AGS, Mills PC. Use of C-reactive Protein in Minimizing Antibiotic Exposure: Experience With Infants Initially Admitted to a Well-Baby Nursery. Pediarics 2000; 106.
  7. Ehl S et al. C-Reactive Protein Is a Useful Marker for Guiding Duration of Antibiotic Therapy in Suspected Neonatal Bacterial Infection. Pediatrics 1997; 99: 216 - 221.
  8. Hofer, N., Müller, W., Resch, B.Non-infectious conditions and gestational age influence C-reactive protein values in newborns during the first 3 days of life. Clin Chem Lab Med, 2011,49: 297 - 302.
  9. Wasunna, A., Whitelaw, A., Gallimore, R., Hawkins, PN., Pepys, MB. C-reactive protein and bacterial infection in preterm infants. Eur J Pediatr, 1990, 149: 424 - 427.
  10. Mathers, NJ., Pohlandt, F. Diagnostic audit of C-reactive protein in neonatal infection. Eur J Pediatr, 1987, 146: 147 - 151.

Documents and materials

Marketing and sales materials

QuikRead go wrCRP Sales Sheet (EN)

QuikRead go wrCRP & wrCRP+Hb Brief Instructions (EN)

QuikRead go Family Brochure (EN)

Info Card on Kits and Controls (EN)


Targeted antibiotic use in primary healthcare


QuikRead go wrCRP Test Procedure Video (EN)


Instructions for use

(For informative use only. Kindly always refer to the latest package insert in the kit.)

QuikRead go wrCRP IFU (FI, SE, NO, DK), 146521, 146522, 152634

QuikRead go wrCRP IFU (GB, DE, FR, IT), 146521, 146522, 152634

QuikRead go wrCRP IFU (NL, ES, EE, LI), 146521, 146522, 152634

QuikRead go wrCRP IFU (CZ, SK, HU, PL), 146521, 146522, 152634

QuikRead go wrCRP Control IFU (GB, DE, FR, ES, IT, CZ, HU, PL, SK, SI, NL, EE, LT, SE, NO, DK, FI), 153038

QuikRead wrCRP Control High IFU (GB, DE, FR, ES, IT, CZ, HU, PL, SK, SI, NL, EE, LT, SE, NO, DK, FI), 153039

Ultrasensitive CRP Conrol IFU (GB, DE, FR, ES, IT, NL, CZ, SK, SI, SE, NO, DK, FI), 68257

Safety Data Sheet

QuikRead go wrCRP SDS (EN)

QuikRead go wrCRP Control SDS (EN)

QuikRead go wrCRP Control High SDS (EN)

Frequently asked questions

I would like to start using the QuikRead go wrCRP tests. Which instrument software version I need on my QuikRead go instrument?
You should have the version 7.5.1.

I have updated my QuikRead go instrument into version 7.5.1 to start using the QuikRead go wrCRP test. However, now I noticed I have still some QuikRead go CRP kits in fridge. Can I use these kits still after the software update?
Yes, in addition to the QuikRead go wrCRP tests, you can use the QuikRead go CRP and QuikRead go CRP+Hb kits with the QuikRead go instrument software version 7.5.1.

I accidentally left a QuikRead go wrCRP kit at room temperature for a weekend. Can I still use it?
Yes, you can use the kit. The unopened kit can be stored at cool or room temperature (2 - 25 ºC) until the expiry date marked on the kit label. After the first opening of the kit components, the cuvettes can be kept at room temperature (18 - 25) for 3 months. The reagent caps for 6 months. See more information in the package insert.

What happens if I accidentally use the 20 µl capillaries with the QuikRead go wrCRP test?
It is important to use only the 10 µl capillaries with orange stripe, which are inside the QuikRead go wrCRP test kit. The 20 µl capillaries have a blue stripe and are to be used with QuikRead go CRP test only. The instrument measures the haematocrit value and above the upper limit (75%), it will not give results. If you dispense twice the amount of sample, the instrument thinks the haematocrit value is double what it actually is. The HCT correction is able to correct only those sample results, which have hematocrit below 37.5%.

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