Quality is built into every stage of our operations through defined processes, analytical testing and systematic controls that support consistent API and pharmaceutical intermediate quality.
Our Quality Control laboratory is equipped with analytical instruments including HPLC, GC-HS, FTIR, UV Spectrophotometer, DSC, stability chambers, colorimeter and microbiology facilities. These capabilities support testing and evaluation across different stages of manufacturing.
Our quality team includes trained and experienced professionals who work with defined procedures and quality systems. Raw materials, in-process samples and finished products are evaluated through appropriate testing before release. Quality checks are carried out at important stages of the manufacturing process to monitor product characteristics and maintain consistency. Analytical results and process observations support informed quality decisions throughout production.
Our approach combines laboratory testing, process monitoring and documentation to maintain control over product quality. This structured system helps ensure that manufactured APIs meet their defined specifications before they are released from the facility.
Defined quality systems and controlled procedures support consistent standards across our manufacturing operations.
Analytical testing and trained professionals support the evaluation of raw materials, in-process samples and finished APIs.
Documented procedures and established quality practices help maintain required standards throughout manufacturing and testing activities.
Continuous monitoring and systematic review help maintain consistent product quality from process evaluation through final release.
At Livmore Life Sciences, our quality testing capabilities support accurate product evaluation through analytical methods, stability studies, microbiological testing and experienced quality professionals.
Our laboratory capabilities support detailed analysis of raw materials, in-process samples and finished APIs using established analytical methods.
Stability studies help evaluate product quality over defined storage conditions and support an understanding of product behaviour throughout its shelf life.
Dedicated microbiological facilities support applicable testing requirements and help evaluate products and manufacturing environments where required.
Our trained quality professionals manage testing, documentation and evaluation activities with attention to defined procedures and product requirements.
Advancing Healthcare Through
Science & Innovation
Survey No. 424, 431, Nana Fofaliya Road,
Vill. Ganpatpura, Karjan, Vadodara - 391210 (Guj.-Ind)
