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Lairus Pharma Manufacturing

Lairus Pharma's well-planned and state-of-the-art facilities have led to its accelerated growth in the pharmaceutical sector. Infrastructure plays a key role in the development and growth of a company. Our company's reputation is built on manufacturing and research and development facilities that are designed to meet global standards and strict quality standards that ensure we deliver only the best products. A production block for high-volume products is available in a cGMP environment. Our site has a well-designed utility system that ensures a regular supply of steam, electricity, chilled water and RO water. Our facilities are equipped with process compliant manufacturing equipment’s such as SSR, GLR, dryer, and centrifuges etc. Additionally, the Quality Control and Quality Assurance departments support the manufacturing facility. We have a well-established system, process, organization structure and technology for producing and delivering quality products. Our customer compliant manufacturing facility satisfies customers to all their needs relevant to manufacturing Intermediates, Speciality chemicals and API’s. The entire system is designed to prevent cross-contamination and mix-ups and to meet regulatory requirements.

The installed equipment allows for a wide range of process variables to operate in accordance with current good manufacturing practice (cGMP) requirements

CRAMS

Lairus Pharma's Contract Research and Manufacturing Services (CRAMS) includes a suite of services for proprietary synthesis, process R&D, scale-up, manufacturing of advanced intermediates, key building blocks, and NCEs from early stage development to the commercialization phase. With its integrated R&D, technology and engineering capabilities, Lairus Pharma has served as a reliable manufacturer to leading innovators and several Global Pharma companies by developing cost-effective and non-infringing processes for various Advance Intermediates.

Quality control

Quality control laboratory performs analysis for initial release of raw material, in-process testing and final release testing of finished product with certificate of analysis. Quality control laboratories develop analytical methods and validate methods, as well as provide support for working standards, impurity analysis, and so on. The well-equipped laboratory consists of modern instrumentation such as HPLC, GC, UV, IR and several others • Complying with ICH guidelines, our quality control laboratory conducts all types of stability studies including long-term, intermediate and accelerated studies. Our QC laboratories have highly trained and qualified chemists.


Our core competencies are

  • • Development and validation of analytical methods
  • • Prepare complete specifications for raw materials, key starting materials and intermediates.
  • • Develop chiral methods.
  • • Conduct a stability study for DMF intermediates and key starting materials in accordance with ICH guidelines.
  • Continuous Improvement

    Lairus Pharma give scope for continuous improvement by various aspects like system, process, technology and quality for innovation of products as per current market requirement. Our continuous improvement strategy always produces best products for satisfying customers need.