Global GxP Auditing
& Quality Assurance
Ensure compliance for your supply chain with our expert GMP, GDP, GCP, and GLP audits. Available globally, on-demand.
Comprehensive Quality Services
GMP Audits
Good Manufacturing Practice audits for API, finished formulations, excipients, and packaging materials.
- • ICH Q7 compliance
- • 21 CFR Part 210/211
- • EU GMP Guidelines
GDP Audits
Good Distribution Practice audits for warehouses, logistics providers, and cold chain transport.
- • Storage conditions verification
- • Transport validation review
- • Security assessment
GCP/GLP/GPvP
Specialized audits for clinical trials (CROs), laboratories, and pharmacovigilance systems.
- • Investigator site audits
- • Bioanalytical lab audits
- • PV system master file review
Third-Party Audits
Independent supplier qualification audits conducted on behalf of marketing authorization holders.
- • Unbiased assessment
- • Cost-sharing models
- • Detailed CAPA follow-up
Regulatory Support
Consulting for regulatory inspection readiness (FDA, EMA) and mock inspections.
- • Gap analysis
- • Staff training
- • Documentation review
Ready GMP Reports
Skip the wait. Access our library of completed audit reports for instant supplier qualification.
Browse LibraryWhy Pharmaqensure?
Global Experience
Auditors located in key pharmaceutical hubs (India, China, Europe, USA) to reduce travel costs and timelines.
Cost-Effective & Fast
Streamlined processes and digital reporting tools ensure you get your report within 10 days of the audit.
Comprehensive Reporting
Our checklist-based reports leave nothing to ambiguity. Clear observations, classifications, and evidence.