PCI provides 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 sterile injectables, highly potent and non-potent drug products.
Our strength lies in the integrated nature of our services, combining 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.
Utilizing our state-of-the-art facilities, we offer unrivalled capabilities and a true focus on customer need. We provide clinical manufacturing of multiple dosage forms for investigational use including solid oral dose, liquids, semi-solids and sterile fill-finish processing.
Our global network of facilities providing clinical manufacturing and packaging services are fully supported by a dedicated and experienced team of Qualified Persons, full analytical laboratories and GMP compliant warehousing services.
Our dedicated team of specialists will be happy to discuss any of your Clinical Trial Manufacturing and Packaging needs. Contact us on +1 779-208-1819 (US) or +44 1495 711 222 (UK/EU) or email firstname.lastname@example.org
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