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ASQ CPGP Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Production Systems | 23%-27% | - Manufacturing operations
|
| Materials Systems | 13%-17% | - Material controls
|
| Packaging and Labeling Systems | 5%-9% | - Packaging controls
|
| Facilities and Equipment Systems | 18%-22% | - Facilities
|
| Quality Management Systems | 22%-26% | - Quality systems
|
| Laboratory Systems | 10%-14% | - Laboratory operations
|
ASQ Certified Pharmaceutical GMP Professional Sample Questions:
1. Automated inspection processes must be:
Response:
A) Conducted manually first
B) Less prioritized than manual inspections
C) Validated
D) Based on staff preference
2. Closed computerized systems are defined by their:
Response:
A) Ability to operate on an open internet platform without security
B) Use exclusively in social networking contexts
C) Inability to process data efficiently
D) Lack of connectivity with other systems and controlled access
3. Contamination controls in filling operations are designed to prevent:
(Select two)
Response:
A) Microbial contamination
B) Physical contamination
C) Financial losses
D) Operational delays
4. Seal tests are developed to inspect __________ of filled and packaged materials.
Response:
A) integrity
B) weight
C) price tags
D) color consistency
5. What action is crucial when receiving materials from unapproved suppliers?
Response:
A) Automatically approve the supplier for future shipments
B) Immediately use the materials in production without further inspection
C) Discard the materials without documentation
D) Take appropriate action such as quarantine and notify the quality department
Solutions:
| Question # 1 Answer: C | Question # 2 Answer: D | Question # 3 Answer: A,B | Question # 4 Answer: A | Question # 5 Answer: D |
