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Comprehensive
Dosage Form Capabilities

Austex Pharma delivers high-quality pharmaceutical formulations across a diverse range of dosage forms, designed for global markets and patient needs.

500+ SKUs Managed
WHO-GMP Certified Facilities
The Standard of Excellence

Our manufacturing capabilities are designed to support a wide spectrum of dosage forms, ensuring flexibility, precision, and compliance across therapeutic categories and markets.

Formulation Portfolio

Precision-focused delivery systems tailored for maximum therapeutic efficacy.

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Tablets

Precision-engineered solid dosage forms designed for stability and effectiveness.

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Capsules

Encapsulated formulations ensuring accurate dosing and patient compliance.

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Syrups / Liquid Orals

Palatable and effective liquid formulations for diverse patient groups.

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Suspensions

Uniform and stable suspensions for controlled delivery.

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Injectables

Sterile, high-quality formulations for critical therapeutic applications.

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Powders / Sachets

Flexible and convenient formats for varied dosing needs.

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Ointments / Topicals

Targeted formulations for localized treatment and skin absorption.

Integrated Manufacturing Excellence

Our facilities leverage high-speed automated lines and closed-system processing to ensure absolute sterility and batch-to-batch consistency. We integrate real-time monitoring and advanced filtration systems to meet the most stringent pharmaceutical standards.

check_circle Fully automated blister and strip packaging
check_circle Closed-loop liquid processing units
check_circle Advanced HVAC with H14 HEPA filtration

Lifecycle of Precision

From concept to global distribution, every phase is governed by scientific rigour.

01

Formulation

Initial blending and active ingredient optimization.

02

Testing

In-process checks for density, viscosity, and potency.

03

Validation

Compliance verification against Pharmacopoeia standards.

04

Manufacturing

Scalable production in GMP-controlled environments.

05

Packaging

Secure, tamper-evident and climate-stable finishing.

Advanced R&D Framework

Our scientists focus on the frontier of bioavailability and stability, ensuring every dosage form performs at its peak when it reaches the patient.

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Bioavailability Optimization

Innovative carrier systems to enhance the solubility and absorption of challenging compounds.

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Stability Testing

Accelerated and real-time ICH stability studies across all climatic zones.

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Analytical Methods

Validated HPLC and GC methods for impurity profiling and assay testing.

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Global Compatibility

Formulations designed for US-FDA, EU-GMP, and PICS regulatory readiness.