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Depyrogenation (P3.160)
Contributed by: Suarez
  • 1. The depyrogenation (dpy) process of glassware and reusable devices must be done
A) prior to each use in sterile compounding
B) once weekly
C) 1
D) biweekly
E) once per month
  • 2. To verify each depyrogenation cycle and it's efficacy
A) use endotoxin challenge vial after depyrogenation commissioning
B) use chemical integrator
C) all options are correct
D) repeat process every 6 months
  • 3. Which type of glassware and/or reusable devices may be placed in the depyrogenation oven?
A) none since everything comes sterile
B) only glassware or devices that can withstand 250 degrees celcius
C) all glassware that will be used for compounding
  • 4. Excluding warm up or cool down times, the dpy process be done:
A) at 375 degrees for 30 minutes or more
B) 2-3hrs at 250 degrees
C) at 250 degrees for 30 minutes or more
D) at 250 degrees for couple of seconds is sufficient
  • 5. Regarding chemical integrator
A) must clearly indicate that desired critical conditions were reached
B) must be the appropriate integrator for depyrogenating
C) all options are correct
D) must be placed in the hardest to heat location within oven
  • 6. When verifying results of dpy cycle, the baked and unbaked vials must have a difference of 1000 fold reduction in endotoxin units.
A) true
B) false
  • 7. After placing temperature probes at the specified test sites for dyp or mimicking such process, the next steps include
A) ensure the difference in temperature between each test site and the set temperature is less than +,- 20 degrees
B) all options are correct
C) try to remember temperature measurements by repeating them more than 3 times
D) start dpy cycle and allow oven to warm up
  • 8. A chemical integrator is a reusable technology that confirms in a quantitative manner in response to a combination of several critical sterilization parameters
A) true
B) false
  • 9. A chemical indicators a disposable technology that confirms in a non-quantitative manner that a given temperature was reached inside of sterilization chamber
A) true
B) false
  • 10. What corrective measures must be taken if the endotoxin challenge vial does not reach a 3-log (1000 fold) reduction in endotoxin units?
A) ensure dyp oven is not used for further dyp until cycle efficacy has been verified
B) repeat process
C) all options are correct
D) contact vendor for appropriate corrective actions when necessary
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