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ASQ CPGP Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Quality Management Systems | 22%-26% | - Quality systems
|
| Packaging and Labeling Systems | 5%-9% | - Packaging controls
|
| Materials Systems | 13%-17% | - Material controls
|
| Laboratory Systems | 10%-14% | - Laboratory operations
|
| Production Systems | 23%-27% | - Manufacturing operations
|
| Facilities and Equipment Systems | 18%-22% | - Facilities
|
ASQ Certified Pharmaceutical GMP Professional Sample Questions:
1. When assessing controls over supplier selection, what is considered a best practice?
Response:
A) Ensuring there are formal contracts or quality agreements in place
B) Choosing suppliers based on geographic proximity only
C) Relying on supplier self-assessment reports without verification
D) Selecting suppliers based solely on cost
2. Automated inspection processes must be:
Response:
A) Conducted manually first
B) Validated
C) Less prioritized than manual inspections
D) Based on staff preference
3. Packaging line setup instructions are crucial for:
Response:
A) Entertainment purposes
B) Making the workplace more colorful
C) Reducing the need for skilled labor
D) Ensuring correct assembly of components
4. What is a required element in both master and batch records?
Response:
A) Marketing strategies
B) Yield calculations
C) Future product development plans
D) Personal employee information
5. What action should be taken for materials received with missing documentation?
Response:
A) Quarantine the materials until the documentation is reviewed and approved
B) Use the materials for non-critical applications only
C) Proceed with using the materials, assuming documentation is not critical
D) Discard the materials immediately without further verification
Solutions:
| Question # 1 Answer: A | Question # 2 Answer: B | Question # 3 Answer: D | Question # 4 Answer: B | Question # 5 Answer: A |
