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Dedicated to Oral Solid Dosage Excellence

Our Manufacturing unit is dedicated to oral solid dosage forms, specialized and dedicated exclusively to the high-volume, quality-driven production of Tablets, Capsules, and Pellets. We are committed to operational efficiency and delivering OSD products that meet the highest global standards for safety, efficacy, consistency and Regulatory-grade quality for both domestic and international markets.

Auxillion aims to be a reliable manufacturing partner for tablets, capsules and pellets that are ready to support current needs and future regulated-market opportunities.

Core Manufacturing Capabilities

We focus exclusively on oral solid dosage forms to achieve depth rather than just breadth:

Tablets

Conventional, film-coated and specialised tablets in multiple strengths and pack formats.

Hard Gelatin Capsules

Capsules filled with powders, granules or pellets.

Pellets & Multiparticulate

High-quality pellets that can be filled into capsules or used in other presentations.

High-Class Facilities & Specialized Capacity

Our manufacturing sites are purpose-built and state-of-the-art, focusing on streamlined OSD production:

Dedicated OSD Units

We operate isolated, high-capacity manufacturing suites equipped with modern compression, encapsulation, and pelletizing machinery to prevent cross-contamination and maximize output.

Advanced Technologies

We utilize validated processes tailored for OSD performance, including Direct Compression, Wet and Dry Granulation, and advanced techniques for creating functional pellets and bi-layer tablets.

Environmental Control

Facilities feature advanced HVAC systems with sophisticated filtration and air pressure management, ensuring a classified environment essential for maintaining the stability and purity of sensitive pharmaceutical powders.

Unwavering Regulatory Compliance

Quality is not just a standard; it is the fundamental operating principle governing every stage of our OSD production.

Global cGMP Adherence

Our operations are meticulously governed by a robust Quality Management System (QMS) that strictly complies with current Good Manufacturing Practices (cGMP) guidelines, including standards necessary for international export.

Validation and Qualification

All critical processes, utilities (purified water, compressed air), and equipment are subject to stringent Installation, Operational, and Performance Qualification to guarantee consistent performance and batch-to-batch reproducibility.

Quality & Compliance Highlights

  • Robust in-process controls at critical stages (granulation, compression, encapsulation, coating and packing)
  • Cleanroom practices and controlled environments tailored for oral solid production
  • Comprehensive documentation and batch traceability to facilitate audits, regulatory submissions and partner requirements
  • A culture of continuous improvement, training and periodic validation to keep systems and processes updated with evolving guidelines

End-to-End Operational Excellence

We integrate modern operational systems to ensure product security, traceability, and market readiness:

Serialization & Traceability

Equipped with advanced serialization technology for product tracking and authentication, meeting global regulatory requirements for anti-counterfeiting.

Packaging Engineering

High-speed, automated packaging lines (blister/strip). Materials selected based on stability testing for optimal protection in various climatic zones.

Continuous Improvement

Utilizing Lean Manufacturing principles and data analytics to optimize throughput, minimize waste, and enhance efficiency without compromising quality.

Partner-Focused, Future-Ready

By concentrating our in-house capabilities on tablets, capsules and pellets, we are able to offer:

Consistent Supply & Scalable Capacity Flexibility in Strengths & Branding Foundation for USFDA/EU Projects

Whether for our own brands or for strategic partners, every product manufactured under the Auxillion name is intended to reflect the same promise: high-class facilities, regulatory-compliant processes and trustworthy quality in every dose.