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ASQ CPGP Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Quality Control and Laboratory Systems | - Testing and release systems
|
| Pharmaceutical Quality Systems | - Quality system principles and implementation
|
| Documentation and Data Integrity | - GMP documentation practices
|
| Validation and Qualification | - Validation lifecycle
|
| GMP Regulations and Compliance | - Inspection readiness
|
| Production and Process Control | - Manufacturing operations
|
ASQ Certified Pharmaceutical GMP Professional Sample Questions:
1. Which of the following are included in the validation and qualification process for new equipment in a pharmaceutical facility?
(Choose two)
Response:
A) Aesthetic Qualification (AQ)
B) Social Media Qualification (SMQ)
C) Design Qualification (DQ)
D) Operational Qualification (OQ)
2. Which of the following is an example of a critical quality attribute?
Response:
A) The color of the tablet coating
B) Sterility for injectable products
C) The font used on the product label
D) The product name
3. Validation studies for aseptic processing must include:
Response:
A) Temperature controls
B) Process simulations (media fills)
C) Annual sales forecasts
D) Taste testing
4. Biological agent traceability requirements are crucial to ensure:
Response:
A) Easy advertisement
B) The fastest production time
C) The lowest production costs
D) Compliance with health and safety standards
5. Quality unit (site) management responsibilities include:
Response:
A) Ensuring proper batch release
B) Organizing team-building events
C) Designing product packaging
D) Setting sales targets
Solutions:
| Question # 1 Answer: C,D | Question # 2 Answer: B | Question # 3 Answer: A,B | Question # 4 Answer: D | Question # 5 Answer: A |




