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Description
In drug manufacturing, QA or QC under GMP rules, ASQ's CPGP shows you understand good manufacturing practice across the product lifecycle. The practice test walks you through quality systems, sterile and nonsterile manufacturing, lab controls, filling and packaging, and GMP regulations. You'll need five years of relevant experience, three of them with decision-making authority.
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CPGP Questions
Study from 110 practice questions aligned to the latest CPGP objectives.
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CPGP is part of the ASQ certification pathway. See how this exam connects to your long-term career goals.
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Frequently asked questions
Everything you need to know about prepping for CPGP.
What is the CPGP exam format?
What topics are on the CPGP exam?
- Quality Systems (17.33%)
- Sterile and Nonsterile Manufacturing Systems (14.67%)
- Laboratory Systems (13.33%)
- Filling, Packaging, and Labeling (12%)
- Regulatory Agency Governance (11.33%)
- Infrastructure: Facilities, Utilities, and Equipment (11.33%)
- Materials and Supply Chain Management (11.33%)
- Product Development and Technology Transfer (8.67%)
How should I prioritize the CPGP syllabus?
What are the prerequisites for CPGP?
How to study for the CPGP exam?
- Study tips:
- Use the official CPGP Handbook (3rd Edition) as your primary open-book reference - it is specifically aligned to the 2023 BoK
- Focus heavily on Quality Systems (Domain II) as it has the most questions (26 scored) and highest weight (17.33%)
- Understand the differences between US FDA, EU, WHO, and other regulatory frameworks as the exam tests global GMP knowledge
- Practice applying ICH guidelines (Q7, Q8, Q9, Q10, Q12) to real-world scenarios
Is the CPGP exam active in 2026?
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