Global Pharma QA
What they do
Global Pharma QA describes independent GLP and GCLP auditing, consultancy, training, and inspection preparation, covering OECD GLP, FDA 21 CFR Part 58, and 21 CFR Part 11. Its public materials present audit services for labs seeking formal GLP readiness.
GLP services
- GLP/GCLP audits
- Inspection preparation
- OECD GLP compliance
- FDA 21 CFR Part 58 compliance
- 21 CFR Part 11 / data integrity
Best fit
Best for: Labs aligning to both OECD GLP and FDA 21 CFR Part 58 requirements.
Consider: Confirm auditor credentials and on-site audit capacity in the proposal.
Official website: www.globalpharmaqa.com
Questions to ask this firm
Is Global Pharma QA a GLP certification body?
No — and neither are we. Nobody on this page can grant GLP compliance status; that comes from national GLP monitoring authorities. Global Pharma QA provides services that prepare a lab for GLP recognition or audit existing programs.
What should I ask Global Pharma QA before signing?
Who will staff the audit (names and credentials), what exactly is in scope (facility / study / data / report), what the deliverable looks like, and what happens if findings need remediation — plus travel and expenses.
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