Sterile Compounding Module 1 Practice Test

These questions are part of the practice quiz. Start practicing

• In which subtype of BSC Class II is all of the work surface area exhausted outside?
• What is a crucial aspect of maintaining sterility in compounded preparations?
• A medication must be compounded in a ____________ environment to be delivered parenterally.
• Which ISO class represents the cleanest environment for compounding sterile preparations?
• Which device can be changed based on airflow and is used for preparing nonhazardous drugs?
• What is the minimum ISO classification necessary for a buffer room?
• In which situation is it inappropriate to use a closed system transfer device?
• When cleaning the PEC, what is important regarding the technique used with cleaning strokes?
• Which type of BSC Class II is typically associated with the highest level of safety for working with biological agents?
• What is the purpose of a vented needle when withdrawing from a vial?
• Which of the following is NOT a standard requirement for the ante area in an SEC?
• Which feature of adaptable systems primarily enhances the workflow of pharmaceutical preparation?
• What is the primary feature of a closed system transfer device (CSTD)?
• What is the significance of the compounding area’s humidity level?
• How far inside the outer edges of a laminar airflow hood must all manipulations be performed?
• In the use of multi-dose vials, what must be avoided particularly for pediatric patients?
• What is one factor that could lead to the need for recertification of a facility?
• USP Chapter ____________ relates specifically to bacterial endotoxin tests.
• What is one of the enforceable requirements of USP Chapter 797?
• What is the primary function of a laminar airflow workbench in sterile compounding?
• Which of the following is NOT a type of sterile compounding facility?
• Which of the following compounding categories has the longest BUD?
• What equipment is used to transfer solutions directly from one container to another?
• Which type of parenteral product is beneficial for hospitals with limited pharmacy operation hours?
• Which category includes CSPs prepared in an ISO class 5 environment but in an uncontrolled space?
• When should 70% Isopropyl Alcohol (IPA) be applied in relation to initiating compounding?
• Which element is critical for preventing microbial growth in controlled environments?
• In accordance with the updates made to USP 797 in 2020, how often should air sampling for Category 3 be done?
• What type of needle presents a smaller lumen?
• Which term describes the substances used to reconstitute or dilute medications based on compatibility and patient factors?
• What is the minimum number of air changes per hour required in the buffer area of an SEC?
• Which of the following is a disadvantage of adaptable systems?
• Which organization is indicated by the abbreviation TJC?
• Which category does a CSP fall into if its BUD may be greater than 12 hours at controlled room temperature?
• Which syringe type should not be used for parenteral administration?
• In relation to air sampling for Category 1 and 2 CSPs, how often should this be performed?
• What should be taken into account when determining the volume of diluents used in medication preparation?
• Which area should have a greater air change rate, the buffer area or the ante area?
• What is the main purpose of having a negative pressure buffer area in hazardous drug preparation?
• What is a requirement for hazardous drug preparation in a Sterile Compounding Environment?
• What is the purpose of overlapping strokes when cleaning the PEC?
• Which chapter sets requirements for storage and transport of compounded preparations?
• What type of pressure is described by a room where the pressure is higher in the treated area?
• During compounding, what is a critical step to ensure safety when handling high-risk level CSPs?
• What is the purpose of determining a beyond use date for a CSP?
• Which subtype of BSC Class II indicates that most of the work surface area is exhausted outside?
• Which type of syringe is characterized by threads that attach to a needle or tubing?
• What type of BSC is known for providing maximum protection and is not commonly used in pharmacy practice?
• Which chapter provides guidelines for the maintenance of sterility in compounded sterile preparations?
• Which factor is essential in designing a sterile compounding environment?
• What is one of the main purposes of engineering controls in sterile compounding?
• Which equipment can measure fluid volume via syringe attachment?
• Which component is integrated into IV tubing to enhance safety for patients?
• What type of cleaning agent is used to remove dirt, debris, microbes, and residuals from the PEC?
• Which category represents CSPs that are the most controlled and have the longest BUD?
• In sterile compounding, how should cleaning supplies be handled inside the hood?
• Which of the following is NOT a common parenteral route?
• What must the verifying pharmacist check for when verifying compounded sterile products?
• CSPs prepared in an ISO class 5 environment with a classified cleanroom suite fall under which category?
• Which task is specifically required when preparing compounded sterile products (CSPs)?
• Which date is assigned by the manufacturer of the medication?
• How frequently are surface samples required to be taken from the hood in a Category 1 CSP preparation?
• What is essential for separating hazardous drug preparation areas in an SEC?
• What is the maximum volume for small volume parenterals?
• Which item is noted for its disposable, flexible properties and is easier to store?
• What describes the efficiency of a HEPA filter during compounding?
• HEPA filters are designed to remove particles as small as what size?
• What supply is used to prevent particles, air, microorganisms, and endotoxins from being infused into patients?
• In which scenario would additional certification of the facility and engineering controls be needed?
• What must be considered while establishing the beyond use dating for compounded sterile preparations?
• What category would a CSP fall into if it is prepared under the least controlled conditions?
• What is the purpose of humidity control in sterile compounding rooms?
• What defines the point after which a Compounded Sterile Product (CSP) should not be used?
• Which chapter encompasses guidelines to prevent harm from excessive bacterial endotoxins?
• Which USP Chapters are considered enforceable?
• What should be ensured to maintain the effectiveness of a laminar airflow workbench?
• Which practice is essential before compounding any sterile product?
• Which factors contribute to the beyond use dating for Category 1?
• What type of container is described as a glass container with injectable solutions that is single use only?
• Which container is identified as holding freeze-dried sterile powder for reconstitution?
• In sterile compounding, what is meant by 'first air' in the context of critical sites?
• What is one of the key components in cleaning and disinfecting to minimize contamination?
• Which syringe type is specifically designed to prevent needle disengagement during administration?
• What is the primary focus of USP Chapter 797?
• In the context of Sterile Compounding, what does the acronym ACPH stand for?
• What is a key characteristic of Category 1 CSPs?
• Which of the following is NOT a contributing factor for Category 3 beyond use dating?
• What measure is important when labeling compounded sterile products?
• What is the BUD for Category 1 compounding?
• What is the minimum number of air changes per hour required in a hazardous drug compounding area?
• What is a primary reason for enforcing strict guidelines in sterile compounding?
• What is the recommended temperature for the room used in sterile compounding?
• What type of container requires a filter needle for access?
• What characteristic of an ampule limits its use after opening?
• Larger filter sizes in in-line filters are specifically used for administering which medications?
• What is a primary characteristic of Category 3 CSPs?
• In the state of Florida, what is the technician-to-pharmacist ratio for sterile compounding?
• Which class of Biological Safety Cabinet (BSC) is designed primarily to protect the user and the surrounding area?
• What should be applied inside the Primary Engineering Control (PEC) immediately before initiating compounding?
• What factors contribute to beyond use dating in Category 2?
• How frequently should sporicidal agents be used?
• What is the maximum allowed humidity in the room for sterile compounding?
• How does a laminar airflow workbench primarily protect the product during compounding?
• Which equipment features an additional HEPA filtration and provides higher air velocity for safety?
• What does manipulating sterile products aseptically help to ensure?
• How many air changes per hour are required in the ante area, assuming it is classified as ISO class 8?
• In terms of sterile compounding, what does 'admixing' refer to?
• Which practice is vital for maintaining sterile conditions during compounding?
• In the context of a laminar airflow workbench, what does interference with filtered air flow lead to?
• Why is it critical to maintain a temperature of 20C or cooler in a sterile compounding environment?
• Which type of drugs are compounded in a positive pressure room?
• Which subtype of Class II BSC is characterized by recirculating all work air?
• What is the key feature of a compounding aseptic isolator (CAI)?
• Which type of compounds does a laminar airflow workbench protect?
• What is a key requirement for environments where sterile preparations are compounded?
• What is a required practice when preparing compounded sterile preparations?
• What does USP Chapter 797 relate to?
• What type of filter must be used for hazardous drug preparation?
• What is the primary goal of the organization responsible for establishing standards for compounding sterile preparations?
• What is the minimum volume for large volume parenterals?
• What does the expiration date indicate in relation to a medication?
• Which USP Chapter is associated with sterility testing?
• What is an example of primary engineering control in hazardous drug compounding?
• What is essential regarding the rubber closure on a vial?
• Which of the following is NOT a characteristic of a positive pressure room?
• What is used to prevent the release of aerosols, vapors, and droplets in sterile compounding?
• What is the minimum ISO classification necessary for an anteroom?
• What is the required frequency for surface sampling in Category 3 CSPs according to USP 797?
• Why is accurate calculation important in the verification process of CSPs?
• Which aspect is not a function of a clean room in sterile compounding?
• What environmental aspect is NOT typically monitored in preparing sterile compounds?
• What ISO class is considered the dirtiest?
• What does CMS stand for relating to healthcare?
• What type of drugs are compounded in a negative pressure room?
• What type of products are described as convenient and ready to administer, primarily for emergency situations?
• Which equipment is designed to protect users from exposure to hazardous drugs or vapors?
• In what type of BSC is the airflow control adjusted for handling hazardous drugs?
• Which USP Chapter focuses on safe handling methods for hazardous drugs?
• Which of the following best describes the air quality requirement in a buffer area for secure compounding?
• Which factor is least likely to influence the selection of diluents for reconstituting medications?
• Which equipment should always be used when withdrawing solution from an ampule?
• Which material is preferred for its less chemical interactions and ability to be sterilized?
• When objects are incorrectly placed in a laminar airflow bench, turbulence is created how many times the diameter of the object?
• What is one of the responsibilities of compounding personnel according to USP chapter 797 and 800?
• What type of flow does a laminar airflow workbench utilize to protect the sterile product?
• Which device is characterized by being a glove box that operates under negative pressure and is used for hazardous drug preparation?
• What component is essential for maintaining the cleanliness of a Sterile Compounding Environment?
• What is the common use for a Class II BSC Type B2?
• What characteristic is unique to a multi-dose vial?
• Are all cleaning supplies inside the hood required to be sterile according to USP 797?
• What defines sterile compounding?
• What are the goals for facilities and engineering controls to minimize microbial contamination?
• Who is responsible for creating and implementing a training program for personnel?
• How should hazardous drugs be stored in relation to other inventory?
• What is the minimum ISO classification necessary for a Primary Engineering Control (PEC)?
• What is the minimum ISO class required for the buffer area of the SEC?
• What is the BUD for Category 2 compounding?
• What does the abbreviation CSTD stand for in sterile compounding?
• What is the significance of the "beyond use date" in sterile compounding?
• What does not apply to USP Chapters 1000 to 1999?
• In which part of the SEC is the PEC located?
• What is a key aspect of the quality control measures described in USP 797?
• Individuals at higher risk of contaminating the environment must report to whom?
• Which material is represented by the abbreviation PVC?
• How often should certification for facilities and engineering controls be performed after the initial certification?
• What is represented by the abbreviation ADC in pharmacy?
• Parenteral administration is the delivery of medication into the body through routes that circumvent the?
• What device is described as a glove box that includes an ante chamber and can be changed based on airflow for nonhazardous drug preparation?
• What is a characteristic of a Class II Biological Safety Cabinet?
• What is the main focus of USP Chapter 800?
• What is a characteristic of a negative pressure room in a Sterile Compounding Environment?
• What is a primary reason for using a sporicidal agent?
• What is the required number of consecutive passes in visual observation and gloved fingertip sampling of both hands for personnel evaluation garbing?
• What organization publishes standards for identity, quality, strength, purity, packaging, and labeling in pharmaceutical settings?
• What is DEHP an abbreviation for?
• How often should 70% IPA be applied when compounding, unless it's a singular compound?
• Which date applies to all Compounded Sterile Products (CSPs)?
• In a Sterile Compounding Environment, what class is required if the ante area opens into a negative pressure room?
• What should be considered when selecting a BSC type for drug preparation?
• What key component is necessary to adhere to during the compounding process to ensure patient safety?
• Compounding category 1, 2, and 3 CSPs for administration within 4 hours of preparation may be subject to what?
• What is the BUD for Category 3 compounding?
• In sterile compounding, what does PEC stand for?
• What is one critical benefit of using a HEPA filter?
• What is one of the key differences between Category 1 and Category 2 compounding?
• What does the expiration date of a compounded product refer to?
• Which USP chapter focuses on preventing patient harm from microbial contamination?
• Which of the following is NOT an advantage of adaptable systems?
• What is the minimum ISO class requirement for the ante area in a Sterile Compounding Environment (SEC)?
• What is the purpose of using a closed system transfer device?
• How often should the training program for personnel be evaluated?
• For cleaning personnel, when should cleaning occur in relation to shifts?
• When objects are correctly placed in a laminar airflow bench, laminar flow turbulence is created how many times the diameter of the object?
• Which syringe is designed for continuous nebulization via an aerogen pump?
• Which medications must be filtered to prevent complications like crystallization?
• Which chapter outlines the requirements for sterility of Compounded Sterile Preparations (CSPs)?
• How often should PEC cleaning be performed?
• What is one important method to minimize the risk of microbial contamination?
• If a CSP has a Beyond Use Date (BUD) of less than or equal to 12 hours at controlled room temperature, which category does it belong to?
• If a CSP has a longer BUD than Category 2, what category is it classified under?
• Critical sites of vials and syringes must be exposed to what type of filtered air in laminar airflow workbenches?
• What practice helps maintain microbial control in the environment because of human shedding?
• What type of syringe may have the needle disengage if not properly attached?
• Which date is determined and set by the compounder?
• What is the significance of compounding categories in forhold to their sterility protocols?
• Which of the following is a responsibility of compounding personnel defined by USP Chapter 797?
• As the size of a syringe increases, how do the increments of calibration marks change?
• What characteristic of HEPA filters helps maintain compounding area cleanliness?
• Which subtype of BSC Class II describes a system where most of the work surface air is recirculated?
• What category of sterile compounding utilizes nonsterile starting ingredients prepared in an ISO class 5 cleanroom?
• Which factor is critical for ensuring optimal air quality in sterile compounding?
• What type of pressure is required in a hazardous drug compounding room?
• When managing hazardous drug preparations in the SEC, what is critical concerning airflow?
• What does the abbreviation CSP stand for?
• What defines a secondary engineering control in the context of hazardous drug preparation?
• What is the primary function of infusion pumps?
• What primary requirement must a compounding area meet to prevent contamination?
• What does the abbreviation BOP represent in the context of pharmacy?
• What kind of pressure is maintained in a room that prevents contaminated air from leaving the space?
• What item is primarily described as solutions that are administered to a patient?
• In what type of pressure containment does hazardous drug preparation need to be conducted?