Authenticity. Accountability. Excellence. Delivered Globally.

PharmAuthent Global is an independent GMP auditing and compliance consultancy supporting pharmaceutical, biotech, and API/excipient manufacturers in meeting international regulatory expectations- with no conflicts of interest and no commercial ties to the sites we audit.

What We Do
→ GMP Supplier & Vendor Audits
→ GxP Audits (API, drug product, packaging, laboratory)
→ Mock Regulatory Inspections
→ GMP Compliance Consulting & Gap Remediation
→ CAPA Effectiveness Review
→ Pre-Approval Readiness Assessments
→ Computer System Validation

Standards We Audit Against
EU GMP · USFDA 21 CFR 210/211 · PIC/S · WHO Technical Report Series · ICH Q7-Q8–Q10–Q12 · ISO 9001:2015 / ISO 15378:2017

Why Manufacturers Choose Us
Independent & Unbiased- objective, fact-based findings, every time
Global Reach- audit network across India, Europe, China, Singapore, Japan, the US, and MENA
Risk-Based Methodology- from scope definition through CAPA close-out
Rapid, Flexible Deployment- without compromising audit rigor

We work with MA holders, pharmaceutical manufacturers, API and formulation companies, CDMOs/CMOs, and regulatory-driven organizations worldwide who need a compliance partner they can act on with confidence.

Let's talk about your next audit, inspection readiness assessment, or QMS gap assessment.
audits@pharmauthentglobal.com

PharmAuthent Global

Org chart

Teams

Offices

PharmAuthent Global

Org chart

Teams

Offices

Related companies