1. Indlela yokuhlola: indlela yokuhlanganisa ubuhlalu obuzibuthe obukabili, indlela ye-chromogenic substrate, indlela ye-immunoturbidimetric

2. Izinto zokuhlola: PT.APTT.TT.FIB, HEP, LMWH.PC, PS, izici ezihlukahlukene zokuhlanganisa, i-D-DIMER, FDP, AT-I

3. Isivinini sokuthola: imiphumela yesampula yokuqala phakathi nemizuzu emi-4

♦ Imiphumela yesampula yesimo esiphuthumayo phakathi nemizuzu emi-5

♦Into eyodwa ye-PT izivivinyo ezingama-200/ihora

♦ Izibonelo ezine eziphelele ezingama-30/ihora

♦ Izibonelo eziyisithupha eziphelele eziyi-10/ihora

♦ Izibonelo ze-D-Dimer ezingama-20 ngehora

4. Ukuphathwa kwesampula: Ama-racks esampula angama-30 angashintshwa, anganwetshwa ngokungapheli, asekele ithubhu yokuhlola yokuqala emshinini, noma yisiphi isimo esiphuthumayo, izikhundla eziyi-16 ze-reagent, ezi-4 zazo ezinomsebenzi wokugqugquzela

5. Ukudluliswa kwedatha: kungasekela uhlelo lwe-HIS/LIS

6. Ukugcinwa kwedatha: ukugcinwa okungenamkhawulo kwemiphumela, isibonisi sesikhathi sangempela, umbuzo nokuphrinta