Zero-Defect Quality & Global Accreditations
Every EVVAI Pharma formulation batch undergoes rigorous spectrographic testing before receiving a digital Certificate of Analysis (COA) for hospital and B2B dispatch.
100% Digital COA
Spectrographic HPLC testing & Certificate of Analysis issued for every batch.
WHO-GMP Audited
Partner facilities operate under strict cGMP cleanroom environmental controls.
Serial Lot Traceability
Barcoded blister packaging with trackable serial batch QR codes.
24/7 QA Support
Dedicated quality desk for hospital procurement boards and distributors.
Accreditations & Quality Certifications
Certified by international health authorities for commercial distribution and tender supply.
WHO-GMP Certified Line
World Health Organization StandardZero-defect Good Manufacturing Practices certification for oral solids, syrups, and sterile injectable cleanroom contract lines.
ISO 9001:2015
Quality Management SystemInternationally audited quality management system governing raw material testing, in-process controls, and batch clearance.
US-FDA Compliant Facility
Regulatory Equipment StandardAdvanced equipment validation, electronic batch records (21 CFR Part 11), and aseptic cleanroom environmental controls.
GLP Accredited Analytical Lab
Good Laboratory PracticeIn-house analytical chemistry, HPLC, GC-MS testing, stability chambers, and raw material purity verification for every EVVAI batch.
Halal & Purity Verified
Global Product StandardStrictly verified vegetarian HPMC capsule sourcing and ingredient purity certification for global export markets.
CTD Regulatory Dossiers
Drug Registration DocumentsComplete Common Technical Document (CTD) format filings ready for hospital procurement and health authority approvals.
Request Quality Audit & COA Dossier
Hospital procurement boards & distributors can request official batch test documents directly.
Request COA Document File
Instant verification for hospitals, clinic networks, and wholesale partners.