EVVAI PHARMA SERVICES & SUPPLY

Certified Pharmaceutical Manufacturing, Cold-Chain Logistics & R&D

EVVAI Pharmaceuticals provides comprehensive end-to-end healthcare infrastructure spanning automated WHO-GMP cleanrooms, cold-chain distribution networks, analytical GLP quality testing, and contract formulation.

WHO-GMP

Cleanroom Certified

ISO Class 5 & 7 compounding suites

2°C - 8°C

Cold-Chain Monitored

Real-time thermal data validation

100% Digital

COA Batch Clearance

Verifiable analytical certificates

CTD / eCTD

Regulatory Dossiers

Global export tender qualification

Deep-Dive Capabilities

Detailed Scope of Operations & Technology

WHO-GMP Verified

Pharmaceutical Manufacturing

Cleanroom Compounding

WHO-GMP accredited cleanroom production of high-potency solid oral dosages (tablets, vegetarian capsules), sterile injectables, and respiratory liquid syrups.

Positive-pressure ISO Class 5 & 7 cleanroom suites

High-speed automated blistering, strip & bottle packaging

Aseptic vial & ampoule filling lines with particulate tracking

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Cold-Chain Monitored

Pharmaceutical Distribution & Cold-Chain

B2B Logistics

End-to-end temperature-controlled pharmaceutical distribution supporting hospital networks, retail pharmacy chains, and institutional healthcare tenders.

Temperature-controlled cold-chain preservation (2°C - 8°C & 15°C - 25°C)

Real-time thermal data logging with FEFO batch traceability

Rapid emergency dispatch for critical care ICU formulations

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Digital COA

Quality Assurance & Analytical Testing

GLP Laboratory

In-house GLP accredited analytical laboratories providing comprehensive batch clearance, raw material assays, and 100% verifiable digital COA documentation.

HPLC spectrographic assay and chromatographic validation

In-vitro dissolution, stability chamber & disintegration testing

Automated cleanroom optical particle counter logging

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Therapeutic R&D

Research & Formulation Development

R&D Synthesis

Advanced therapeutic formulation design focusing on active drug substance stability, sustained-release mechanisms, and bioavailability optimization.

Custom delivery systems (enteric, sustained release, effervescent)

Excipient compatibility screening & stability profile validation

Pilot batch development and seamless technology transfer

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GCP Aligned

Clinical Research & Safety Validation

Clinical Trials

Regulatory-compliant therapeutic safety validation and pharmacokinetic profiling aligned with international Good Clinical Practice (GCP) standards.

Phase-aligned pharmacokinetic (PK) and pharmacodynamic (PD) profiling

Bioequivalence evaluation and clinical safety dossier preparation

Regulatory dossier advisory for international tender qualifications

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CMO Scalable

Custom & Third-Party Manufacturing (CMO)

Private Label

Custom formulation scaling, private label production, and turnkey regulatory filing support for domestic and global pharmaceutical brand owners.

Turnkey formulation compounding and custom blister packaging

Flexible batch capacity ranging from pilot batches to bulk commercial volume

Complete CTD / eCTD dossier filings for global marketing approvals

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Institutional & Commercial Partnerships

Partner With EVVAI Pharmaceuticals Today

Whether you require emergency hospital supply, high-volume generic distribution, or private label contract manufacturing, our commercial desk is ready to support your organization.

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