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 unrivaled capabilities and a true focus on customer needs. 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 +1 215-613-3600 (US) or +44 1495 711 222 (UK/EU) or email talkfuture@pci.com
Our Clinical Trial Services
Talk to us about our world leading clinical trial manufacturing and packaging services today.
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