Frequently Asked Questions
The CPGP certification validates your expertise in Good Manufacturing Practices within the pharmaceutical industry.
It’s offered by the American Society for Quality (ASQ), a globally recognized quality organization.
CPGP stands for Certified Pharmaceutical GMP Professional, focusing on compliance and quality systems.
Any professional involved in pharma manufacturing, QA, QC, validation, or regulatory affairs can apply.
Candidates usually need a bachelor’s degree and relevant industry experience in GMP-related fields.
It ensures professionals understand GMP principles, regulations, and quality processes for pharmaceutical production.
The exam consists of multiple-choice questions covering GMP systems, compliance, validation, and documentation.
- You’ll have approximately 4 hours to complete the test.
- Key areas include GMP principles, documentation, risk management, validation, audits, and regulatory compliance.
Use the ASQ study guide, mock tests, and real-world GMP scenarios to strengthen your understanding.
It typically ranges between $400 $550, depending on whether you’re an ASQ member.
You can register directly on the official ASQ website and choose your preferred exam window.
Yes, ASQ offers both online proctored and in-person test center options.
It’s generally conducted twice a year, but check ASQ’s official schedule for updated dates.
You need to achieve a minimum passing percentage as defined by ASQ, usually around 70%.
Yes, candidates can retake the exam during the next available testing window.
You gain career advancement, higher credibility, and global recognition in pharmaceutical quality.
Absolutely! The certification is recognized globally across the pharma and healthcare industries.
It’s valid for three years, after which you must apply for recertification.
You can maintain it by earning recertification units through training, work experience, or professional development.
You can work as a GMP auditor, QA manager, validation specialist, or compliance officer.
Salaries vary by role, but certified professionals often earn 20–30% more than non-certified peers.
It equips you with skills to manage inspections, documentation, and audit preparedness effectively.
You must have a few years of hands-on GMP experience in a regulated pharmaceutical setting.
Use the ASQ Handbook, official prep courses, and online GMP study resources.
Yes, industry experience is crucial for understanding practical GMP implementation.
It demonstrates expert-level knowledge and positions you for leadership or auditing roles in pharma.
Students can prepare, but actual eligibility requires industry experience.
Top employers include pharma manufacturing companies, CROs, QA firms, and regulatory agencies.
- Because it’s a globally respected credential that validates your commitment to pharmaceutical quality excellence.
