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ASQ CPGP Valid Dumps Ppt | CPGP Test Review

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ASQ Certified Pharmaceutical GMP Professional Sample Questions (Q519-Q524):

NEW QUESTION # 519
The main difference between systems and process audits is that systems audits evaluate:
Response:

A. Individual employee performance
B. The process efficiency only
C. The entire quality system
D. The end product quality

Answer: C

NEW QUESTION # 520
Reviewing test methods against compendial requirements is important to ensure:
Response:

A. Only non-compendial methods are used in the lab.
B. The quickest method is chosen for all tests.
C. Compliance with both general and informational compendial chapters as needed.
D. Methods are chosen based on their complexity.

Answer: C

NEW QUESTION # 521
What is the primary goal of sanitization procedures in pharmaceutical manufacturing?
Response:

A. To ensure equipment and facilities meet aesthetic standards
B. To eliminate or reduce microbial contamination to acceptable levels
C. To create a pleasant scent in the manufacturing area
D. To comply with interior design guidelines

Answer: B

NEW QUESTION # 522
Change control for equipment in the pharmaceutical industry ensures:
Response:

A. Continual compliance and maintenance of the equipment's qualified state
B. A diversity of equipment colors to enhance employee morale
C. The equipment matches the latest fashion trends
D. That equipment can be easily swapped out for newer models

Answer: A

NEW QUESTION # 523
What is a critical factor when designing pharmaceutical facilities to minimize the risk of cross- contamination?
Response:

A. The aesthetic appeal of the buildings
B. Availability of recreational areas for staff
C. Proximity to urban areas
D. Separation of areas for antibiotics, hormones, and toxins

Answer: D

NEW QUESTION # 524
......

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