Truelixir Life Science Pvt. Ltd.

Manufacturing Excellence at TruElixir

Manufacturing at TruElixir is driven by a commitment to accuracy, safety, and continuous improvement. Our injectable manufacturing facility is developed to support high-performance pharmaceutical production while maintaining strict adherence to global quality and regulatory standards.

The facility combines modern automation, controlled environments, and experienced technical teams to ensure reliable and efficient manufacturing outcomes. Every stage of production is carefully structured to minimize risk, maintain consistency, and support dependable healthcare delivery.

Through well-defined quality systems and disciplined sterile manufacturing practices, TruElixir ensures that each product meets defined safety and performance parameters. Our processes are designed to support scalability while preserving precision and product integrity.

By integrating technology, operational expertise, and quality-focused workflows, TruElixir continues to strengthen its manufacturing capabilities and deliver pharmaceutical solutions trusted by healthcare providers across multiple markets.

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Controlled & Efficient Production Environment

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Automation-Enabled Manufacturing Operations

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Consistent Quality & Process Reliability

Worldwide Manufacturing

Advanced IV fluid manufacturing using Form-Fill-Seal technology with global quality standards

Best Quality Service

WHO-GMP certified production with strict QA/QC ensuring sterile and safe saline solutions.

Experienced Workers

Skilled professionals supported by modern equipment and controlled sterile facilities.

Advanced Infrastructure

TruElixier operates a modern injectable manufacturing facility equipped with advanced infrastructure and automated production systems designed for precision.

The plant supports sterile manufacturing within controlled environments that maintain safety, consistency, and process reliability.

Integrated equipment, digital monitoring, and streamlined workflows enhance operational efficiency while reducing manual intervention.

This strong infrastructure foundation enables consistent product performance and supports long-term manufacturing excellence.

Sterile Manufacturing

Controlled cleanroom environments ensure sterile production across every stage of injectable manufacturing.

Validated sterilization methods, filtration systems, and environmental monitoring maintain strict contamination control.

Standardized procedures help ensure reproducibility, safety, and compliance with global manufacturing expectations.

These sterile practices reinforce product integrity and strengthen trust in every injectable solution delivered.

Expert Team

A multidisciplinary team of scientists, pharmacists, engineers, and technicians drives manufacturing operations.

Cross-functional collaboration supports efficient problem solving, process optimization, and innovation.

Continuous training programs ensure alignment with evolving technologies and regulatory standards.

The team’s expertise enables consistent quality, operational stability, and sustainable manufacturing growth.

Scalable Production

The facility is designed to support flexible and scalable production across multiple injectable formats.

Automation and modular production lines allow efficient expansion without compromising quality.

Capacity planning and optimized workflows enable faster response to changing customer requirements.

This scalability ensures reliable supply continuity while maintaining strict safety and compliance standards.

Quality Excellence

Our Quality Control (QC) department ensures product safety, consistency, and regulatory compliance through comprehensive testing at every stage — from raw and packaging materials to in-process checks and finished product evaluation. Each batch undergoes detailed chemical and microbiological analysis, supported by stability and shelf-life studies to confirm performance and reliability throughout the product lifecycle.

Quality Control is at the core of our operations, with thorough testing of materials, in-process monitoring, and finished product evaluation. Equipped with state-of-the-art analytical instruments, our labs ensure safety, consistency, and long-term product stability.

Quality Control

Raw materials, packaging materials, in-process samples, and finished products undergo extensive testing.

Quality Assurance

QA oversees washing, sterilization, filling, sealing, and packing to ensure specification compliance.

Analytical Laboratories

Modern instruments support chemical, microbiological, stability, and shelf-life studies.

Process Monitoring

Continuous monitoring systems help maintain consistency, traceability, and operational control.

Harmonized Documentation

Standardized documentation ensures traceability, regulatory readiness, and process uniformity.

Continuous Learning Culture

Corrective and preventive actions strengthen processes and support continuous improvement.

Quality Metrics & Monitoring

Key indicators are analyzed to improve performance, reduce risks, and support decisions.

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