At Cataliq Laboratories, quality is not just a process—it is our commitment. Our WHO-certified facility in Ahmedabad operates under stringent Quality Assurance (QA) and Good Manufacturing Practices (GMP) to ensure that every product reaching patients is safe, effective, and reliable.
Quality Assurance is integrated into every stage of our operations, from vendor qualification and raw material sourcing to manufacturing, packaging, and final product release. Our QA team works independently and oversees all systems to maintain global compliance and continuous improvement.
All finished goods undergo extensive physical, chemical, and microbiological testing before release. Only batches that meet all regulatory and internal quality criteria are approved for dispatch.
Our QA operations are supported by a dedicated Quality Control laboratory equipped with:
We emphasize ongoing training for all employees to ensure adherence to the latest GMP guidelines. Periodic audits, quality reviews, and improvement initiatives help us maintain high performance and compliance levels.
Quality at Cataliq Laboratories is guided by a single principle: patient well-being first. Every decision we make and every process we implement is aligned with this mission, ensuring that our medicines consistently meet global quality standards and bring meaningful value to healthcare
To maintain complete transparency and integrity, Cataliq Labs ensures that Quality Assurance (QA), Quality Control (QC), Production, and Stores function as independent departments, each reporting directly to the Managing Director.
This structure allows for unbiased decision-making, full accountability, and consistent adherence to Good Manufacturing Practices (GMP).
Our Quality Control Department is equipped with advanced physicochemical and microbiological laboratories, managed by highly trained professionals. Every batch of raw materials, in-process goods, and finished products undergoes rigorous testing before release.
The QC department ensures:
By combining modern equipment with meticulous analysis, Cataliq Labs guarantees consistent product quality across its β-lactam and non-β-lactam manufacturing units.
The Quality Assurance team ensures that every manufacturing process adheres to WHO-GMP and regulatory standards. From raw material procurement to packaging and dispatch, QA oversees every step, ensuring that only products meeting approved specifications are released to the market.
The QA team focuses on:
This integrated approach ensures compliance, consistency, and quality integrity at every level.
At Cataliq Labs, quality improvement is a continuous journey. We regularly conduct internal audits, employee training, and facility upgrades to align with the latest technological and regulatory developments.
Our philosophy of continuous learning drives innovation in manufacturing, testing, and documentation, enabling us to consistently deliver world-class pharmaceutical products.
In addition to large-scale manufacturing, Cataliq Labs also conducts formulation development and R&D activities. Though modest in scale, our research facilities play a crucial role in developing new and improved formulations that meet both national and international standards.
This focus on innovation and formulation excellence ensures that we stay ahead in a competitive global market.
Cataliq Labs complies with all statutory and regulatory requirements, ensuring every process meets national and international benchmarks. Our WHO-GMP certified pharma plant in Ahmedabad is regularly audited and upgraded to maintain compliance and performance excellence.
By following a system-driven approach, Cataliq Labs ensures every product reflects its promise of trust, safety, and superior quality.
At Cataliq Labs, quality is not just a target; it’s our tradition.
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