Compounded Sterile Preparations Pharmacy Sample Examination Items

These sample examination items are made available by BPS for the purposes of familiarizing certification candidates and other stakeholders with the structure and format of BPS certification examinations. This is not meant for use as a self-assessment. Performance on any of these items does not correlate with performance on the actual examination.

The content of these examples is meant to be illustrative of actual examination items, but these items do not appear on the certification examination and are not meant to identify the scope of the examination. For a more comprehensive indication of the scope of each certification examination, please refer to the Exam Content Outline for each specialty area.

Examination items are in multiple-choice format. The great majority of examination items are multiple-choice with a single response from among four options. Some examinations may include a small percentage of items that require selection of multiple (three or four) responses from among a larger set of available (up to eight) options. Examinations items may also be supplemented by an image.

A 503A compounding pharmacy at a health-system centralized compounding facility was inspected by the FDA following a complaint. An FDA form 483 was issued to the pharmacy. What is the correct response from the pharmacy?

The findings do not need to be addressed since the FDA's Insanitary Conditions document is just guidance.
The findings do not need to be addressed since the pharmacy is considered a 503A compounder.
The findings must be addressed using a corrective and preventative action plan.
The findings should be addressed using a failure mode and effects analysis.

Correct!

Incorrect!

A hospital pharmacy received a shipment of antineoplastic hazardous drugs. Where should the shipment be unpacked?

A designated area within the pharmacy department with positive pressure relative to the surrounding areas
A designated area within the pharmacy department with neutral or negative pressure relative to the surrounding areas
An area on the delivery truck by the loading dock before transporting to the pharmacy department
An area within the sterile compounding clean room

Correct!

Incorrect!

Which organization regulates disinfectants by evaluating and registering manufacturer data submitted for microbiocidal activity, stability, toxicity, and contact time for labeling indicated uses?

Centers For Disease Control and Prevention
Environmental Protection Agency
Food and Drug Administration
Occupational Health and Safety Administration

Correct!

Incorrect!

When preparing a horizontal laminar airflow workbench for compounding a sterile product, compounding personnel should:

clean and disinfect working surfaces 6 inches from the front and sides of the hood.
only use cleaning materials that are non-shedding.
use povodine-iodine to wipe surfaces clean during heavy surface contamination.
use sterile gauze to wipe working surfaces to prevent damage of the surface areas

Correct!

Incorrect!

Which ingredient is incompatible and must not be added to a 3-in-1 parenteral nutrition admixture?

Iron
Phytonadione
Selenium
Zinc

Correct!

Incorrect!

What is the most appropriate delivery route for a parenteral nutrition formulation with an osmolarity of 1,230 mOsm/L?

Central venous catheter
Midline catheter
Peripheral catheter
Subcutaneous catheter

Correct!

Incorrect!

How often must Category 2 compounding personnel demonstrate proficiency through hands-on testing/evaluation?

Every 3 months
Every 6 months
Every 12 months
Every 18 months

Correct!

Incorrect!

How often must compounding personnel pass gloved fingertip testing and media-fill testing of aseptic work skills when working with sterile ingredients for Category 3 CSPs?

Initially and monthly
Initially and annually every 3 months
Initially and every 6 months
Initially and annually

Correct!

Incorrect!

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Compounded Sterile Preparations Pharmacy Sample Questions

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