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ASQ CPGP Exam Syllabus Topics:

ASQ Certified Pharmaceutical GMP Professional Sample Questions:

1. When an adverse event report involves a counterfeit product, the company should:
Response:

A) Inform regulatory authorities and possibly issue a public warning to prevent further harm.
B) Ignore the report, as it does not involve a genuine product.
C) Consider the event as a minor issue that does not require action.
D) Only inform the direct customers about the counterfeit product.

2. In terms of compendia, required chapters are to informational chapters as:
Response:

A) Outdated is to modern.
B) Complicated is to simple.
C) Expensive is to cost-effective.
D) Mandatory is to optional.

3. The layout of pharmaceutical manufacturing equipment must be designed to:
Response:

A) Ensure that all equipment is visible from the facility's entrance
B) Allow for easy photography and videography
C) Minimize errors and facilitate cleaning and maintenance
D) Reflect the hierarchical structure of the company

4. Which of the following are considered when defining corrective actions?
(Choose two)
Response:

A) Actions to prevent recurrence of the issue
B) Actions to improve employee benefits
C) Actions to address and correct the root cause of a problem
D) Actions to enhance marketing strategies

5. Routine maintenance of air and water filters in a pharmaceutical facility helps to:
Response:

A) Ensure the filters are color-coordinated with the facility interiors
B) Prevent contamination and maintain a controlled environment
C) Decrease the workload on facility staff
D) Impress regulatory inspectors with the facility's cleanliness

Solutions: