BUILT ON ASSURANCE BACKED BY DOCUMENTATION

At Vetex Pharma, quality is not just a requirement — it's a commitment embedded in every decision we make. While we do not manufacture ourselves, we work exclusively with GMP-compliant, audited manufacturers whose systems meet stringent international standards.

From dossier preparation to batch release, we ensure every API or formulation delivered through our network is regulatory-ready, well-documented, and compliant with global norms.

✅ What Quality Means at Vetex

• 🧪 Manufacturer Qualification: All sourcing partners are pre-audited and qualified for GMP compliance (USFDA, EMA, WHO, NMPA, PPB, etc.). We assess every site for quality systems, production capacity, documentation, and ESG responsibility.
• 📋 Regulatory Documentation: Our product offerings are backed by:
  • US DMFs (Type II / Type III)
  • EU CEPs
  • CTD-ready dossiers
  • WHO-prequalified & local registrations (NAFDAC, ANVISA, INVIMA, PPB, SFDA)
• 🧾 Full Traceability: From inquiry to dispatch, every batch is trackable through COA, MOA, BMR/BPR, and stability reports.
• ⚖️ Ethical and Transparent Operations: Every transaction includes clear terms, full documentation, and client-approved specs — no grey zones.

📦 We Ensure

• Product-specific audit summaries
• Compliance with GMP, GDP, SOP protocols
• Consistent batch reproducibility
• Supplier ESG alignment where applicable
• Final product release supported by STP and COA

🛡️ Partnering for Compliance

We act as your quality filter and regulatory co-pilot — ensuring that every product meets the expectations of your local regulatory body before it reaches your facility. Whether you're applying for a dossier submission, tender qualification, or formulation tech transfer, we support you with the required documentation and guidance every step of the way.

🌐 Certified to Deliver

• ✅ USFDA
• ✅ EDQM (CEP)
• ✅ WHO-GMP
• ✅ PMDA / ANVISA / INVIMA / SFDA / NAFDAC
• ✅ ISO 9001 / ISO 14001 / HACCP