1. When should the efficacy of a compounding pharmacy's
cleaning and disinfection procedures be verified?
A. Only when a contamination is detected
B. At routine intervals and after any major environmental changes
C. Once a year
D. Only during FDA inspections
Answer: B) At routine intervals and after any major environmental
changes
Rationale: Regular verification of cleaning and disinfection
procedures is necessary to ensure the environment is consistently
maintained and free from contamination.
2. Which type of equipment is typically used for the sterilization
of compounded sterile preparations?
A. A biological safety cabinet (BSC)
B. A microwave oven
C. An autoclave
D. A UV light chamber
Answer: C) An autoclave
,Rationale: An autoclave is commonly used to sterilize
compounded sterile preparations by using steam under pressure to
kill microorganisms.
3. What is the primary role of the pharmacist during sterile
compounding?
A. To manage inventory
B. To prepare and ensure the accuracy and sterility of
compounded preparations
C. To clean the compounding equipment
D. To handle patient interactions directly
Answer: B) To prepare and ensure the accuracy and sterility of
compounded preparations
Rationale: The pharmacist is responsible for the preparation,
sterility, and accuracy of sterile compounds, ensuring they meet
all safety and quality standards.
4. Which of the following is considered a critical factor in sterile
compounding that ensures the protection of patient health?
A. The speed of drug preparation
B. The sterility of compounded drugs
C. The appearance of the preparation
D. The cost of the compounded preparation
Answer: B) The sterility of compounded drugs
, Rationale: The sterility of compounded preparations is the most
critical factor, as it directly impacts patient safety and health by
preventing infections and other complications.
5. When should a compounding pharmacy use a Class II Biological
Safety Cabinet (BSC)?
A. For preparing non-sterile preparations
B. For preparing sterile preparations with risk of exposure to
hazardous drugs
C. Only for testing new products
D. For packaging non-sterile compounds
Answer: B) For preparing sterile preparations with risk of
exposure to hazardous drugs
Rationale: A Class II BSC is used for compounding sterile
preparations that involve hazardous drugs, as it provides both
containment and sterility assurance.
6. When should personnel perform air quality testing in a sterile
compounding environment?
A. Only when there are visible signs of contamination
B. Once a month
C. At routine intervals and after any major change to the
environment
D. Only before the annual inspection
cleaning and disinfection procedures be verified?
A. Only when a contamination is detected
B. At routine intervals and after any major environmental changes
C. Once a year
D. Only during FDA inspections
Answer: B) At routine intervals and after any major environmental
changes
Rationale: Regular verification of cleaning and disinfection
procedures is necessary to ensure the environment is consistently
maintained and free from contamination.
2. Which type of equipment is typically used for the sterilization
of compounded sterile preparations?
A. A biological safety cabinet (BSC)
B. A microwave oven
C. An autoclave
D. A UV light chamber
Answer: C) An autoclave
,Rationale: An autoclave is commonly used to sterilize
compounded sterile preparations by using steam under pressure to
kill microorganisms.
3. What is the primary role of the pharmacist during sterile
compounding?
A. To manage inventory
B. To prepare and ensure the accuracy and sterility of
compounded preparations
C. To clean the compounding equipment
D. To handle patient interactions directly
Answer: B) To prepare and ensure the accuracy and sterility of
compounded preparations
Rationale: The pharmacist is responsible for the preparation,
sterility, and accuracy of sterile compounds, ensuring they meet
all safety and quality standards.
4. Which of the following is considered a critical factor in sterile
compounding that ensures the protection of patient health?
A. The speed of drug preparation
B. The sterility of compounded drugs
C. The appearance of the preparation
D. The cost of the compounded preparation
Answer: B) The sterility of compounded drugs
, Rationale: The sterility of compounded preparations is the most
critical factor, as it directly impacts patient safety and health by
preventing infections and other complications.
5. When should a compounding pharmacy use a Class II Biological
Safety Cabinet (BSC)?
A. For preparing non-sterile preparations
B. For preparing sterile preparations with risk of exposure to
hazardous drugs
C. Only for testing new products
D. For packaging non-sterile compounds
Answer: B) For preparing sterile preparations with risk of
exposure to hazardous drugs
Rationale: A Class II BSC is used for compounding sterile
preparations that involve hazardous drugs, as it provides both
containment and sterility assurance.
6. When should personnel perform air quality testing in a sterile
compounding environment?
A. Only when there are visible signs of contamination
B. Once a month
C. At routine intervals and after any major change to the
environment
D. Only before the annual inspection