At PCI, the strength lies in the integrated nature of our approach to manufacturing, encompassing non-potent and highly potent drug products including oral solid dose, liquids and semi-solids, sterile fill-finish and lyophilization from development to commercial scale.
Choosing a reliable partner for the development of your product is critical to the success. Our mission is to deliver life-changing therapies to the patients that depend on them through our range of pharmaceutical manufacturing services.
We provide a comprehensive service at each stage of the product lifecycle for a wide range of dosage forms, in full compliance with GMP regulatory standards for both highly potent, non-potent and sterile injectable drug products.
Our integrated service offering that combines formulation and analytical development with GMP clinical manufacturing and packaging through a full cross-functional project team, coordinated by an experienced team of project managers ensures a seamless, end-to-end solution.
Utilizing our state-of-the-art facilities, we offer unrivalled capabilities and a true focus on customer need.
All manufacturing services are fully supported by a dedicated and experienced team of Qualified Persons, full analytical laboratories and GMP compliant warehousing.
Our development & manufacturing services
February 26, 2024
February 13, 2024
February 02, 2024
November 21, 2023