Clinical Trial Manufacturing and Packaging

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 +1 779-208-1819 (US) or +44 1495 711 222 (UK/EU) or email

Talk to us about our world leading clinical trial manufacturing and packaging services today.

Always growing and continually advancing, we support you from early-stage development through commercialization and beyond, and with 6000+ people in 30 global GMP facilities, we are always near.