Prism Life Sciences Ltd.| Home Blueprint: Horizontal Drop-Down Menu

"We at Prism believe that infrastructure is the key to successfully meet the demands of the medical profession world over. And at Prism, infrastructure - excellence is a priority."

The plant at Chattral, Gujarat

Prism's plant at Chattral, Gujarat reflects class. With a state of the art unit and a committed workforce, our production plant has a daily output of 2 million tablets, 1 million capsules and half a million units of external preparation a day. The manufacturing operations are focused on producing generics, branded generics, over the counter products & antiretrovirals in the full range of dosage forms, including tablets, capsules, injectables, ointments, creams & dry syrups. A wide range of regulatory agencies routinely conduct stringent audits of our manufacturing facilities for compliance with good manufacturing practices.

Prism identifies Research & Development as the thrust areas for attaining leadership in the industry. Highly qualified personnel constantly study drugs and explore opportunities to alter the structure, so as to increase efficacy and compatibility. The company tries to reprocess its manufacturing stages by adding new combinations for new products in the markets. 'Refining' is the key process through which the company adds innovations to inventions. Immense studies are carried out on the ingredients and the manufacturing processes of the currently marketed drugs. Thereafter, a series of strategies are drawn on the basis of the findings, and by virtue of cutting-edge expertise and knowledge, innovating a whole new process of manufacturing refines the drug. This ultimately enriches the drug, nevertheless making it cost-effective too, so that it is within the reach of the masses. With the help of its personnel, Prism has been able to introduce novel combinations in the anti-hypertensive, anti-diabetic segments such as triple combination of an ARB + Calcium channel blocker & diuretic (Telmisartan + Amlodipine + Hydrochlorothiazide) and Pioglitazone + Metformin. Many such dosage combinations developed by Prism make it possible for us to add life to livihg in the lives of the people worldwide.

Technology is what makes Prism ride the crest. The reliability of a drug being directly related to the quality of manufacturing process, the company pays maximum attention to technology. For higher productivity, quality and calibre, regular investments in modern machinery are a common practice here. To parallel global expertise and acceptance, the thrust is on imported machines sourced from reputed names in the international league. Even raw materials, though sourced from renowned icons in the industry, go through a multi-check process to ensure unparalleled compatibility and efficacy in the end product. Regular updates on development of new technology around the world are a ritual at Prism. Well defined protocol for installation qualification, coupled with revalidation systems and process validation powers the company with greater advantages in terms of quality and acceptance.

Qualified personnel constantly keep a hawk-eye through the latest quality assurance equipments and stringent quality checks at various levels. So much so that even environmental monitoring and control systems are validated regularly. A quality control laboratory with sophisticated instruments to provide chemical and microbiological analytical support dominates the premises. Various procedures and stringent checks are carried out to maintain the quality. Quality as a law is not only applied to the process of manufacturing, but also extends to the areas of sourcing raw materials and packaging. In fact the priciple of quality-first begins with the company's biggest resource - its people. We look at each day as a chance to invest life into life. A chance to share our experiences and deposit it into someone's else conscience. Each day is a chance to add life to living in the lives of millions of patients worldwide.

We have a highly skilled team of regulatory affairs specialists who are well versed with regulatory policies and procedures and have a vast experience in the timely filing of dossiers as well as handling regulatory queries from both customers and health authorities.