Who is Catalent Lifesciences?

Catalent Lifesciences operates a state-of-the-art, world-class pharmaceutical manufacturing campus. Our facility proudly holds the most stringent global regulatory accreditations, including WHO GMP, EU GMP, USFDA, and UK MHRA, underscoring our unwavering commitment to pharmaceutical excellence.
Established in 2016 under the visionary leadership of Dr. Jessica (M.B.B.S., U.S.A.), Catalent Lifesciences stands as a dynamic and rapidly expanding entity within the pharmaceutical sector. We specialize in the meticulous production and reliable distribution of high-quality finished dosage forms, catering to both domestic imperatives and global healthcare demands.
Our robust foundation is built upon years of profound industry expertise and a comprehensive understanding of intricate worldwide pharmaceutical markets. This strategic positioning fuels our ambitious growth trajectory in both the development and manufacturing of proprietary pharmaceutical products and as a trusted contract manufacturing organization (CMO).
At the core of Catalent Lifesciences lies an uncompromising commitment to "Quality Assurance." This principle is deeply ingrained in every aspect of our operational framework. Through the rigorous implementation and meticulous control of advanced quality management systems, coupled with the dedication of our highly skilled personnel and the deployment of leading-edge technology, we guarantee the consistent quality, absolute purity, assured safety, demonstrated efficacy, and robust stability of our diverse pharmaceutical product portfolio. This encompasses a wide spectrum of critical dosage forms, including sterile injectables, solid oral dosage forms (tablets and capsules), liquid formulations (syrups), and semi-solid preparations (ointments), all manufactured in strict adherence to evolving international pharmacopoeial standards and regulatory advancements..