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ASQ CPGP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Topic 1: Documentation and Data Integrity | - GMP documentation practices
|
| Topic 2: Quality Control and Laboratory Systems | - Testing and release systems
|
| Topic 3: GMP Regulations and Compliance | - Inspection readiness
|
| Topic 4: Production and Process Control | - Manufacturing operations
|
| Topic 5: Validation and Qualification | - Validation lifecycle
|
| Topic 6: Pharmaceutical Quality Systems | - Quality system principles and implementation
|
ASQ Certified Pharmaceutical GMP Professional Sample Questions:
Question 1
What is a required element in both master and batch records?
Response:
A. Marketing strategies
B. Personal employee information
C. Yield calculations
D. Future product development plans
Question 2
What should be done with damaged materials upon receipt?
Response:
A. Quarantine and assess for further action
B. Donate them to charity
C. Use them as if they were undamaged
D. Ignore the damage and proceed with production
Question 3
Regulatory requirements for compressed air and gas systems include all the following EXCEPT:
Response:
A. The color coordination of piping systems
B. Purging requirements
C. Filtration and venting
D. Storage and flow regulation
Question 4
What outcome is expected from conducting thorough APRs and PQRs?
Response:
A. Increase in employee productivity
B. Reduction in manufacturing costs
C. Enhanced regulatory compliance and product quality
D. Identification of new markets
Question 5
Management review of the QMS is crucial for:
Response:
A. Planning corporate events
B. Approving annual leave
C. Tracking stock prices
D. Ensuring continuous improvement
Solutions:
| Question 1 Answer: C | Question 2 Answer: A | Question 3 Answer: A | Question 4 Answer: C | Question 5 Answer: D |





