At MedPharm, our global presence represents more than just geographical reach; it embodies our dedication to serving clients wherever they are, while ensuring scientific continuity, regulatory compliance, and operational efficiency—hallmarks of a world-class Contract Development and Manufacturing Organization (CDMO).
Our facilities are strategically located to support the development, testing, and manufacturing of topical, transdermal, and other complex drug products for partners across North America, Europe, and beyond. Each site is purpose-built and fully aligned with our integrated approach, guaranteeing consistency in quality, communication, and results.
MedPharm proudly collaborates with pharmaceutical and biotech companies across:
We routinely support programs targeting approvals from regulatory bodies such as the FDA, EMA, MHRA, Health Canada, TGA, and other global health authorities.
Integrated Teams Across Sites: Scientific knowledge, project continuity, and decision-making flow freely between locations.
Built for Cross-Border Support: Whether you need clinical supply in the U.S. or development data for an EMA submission, our teams coordinate seamlessly.
Unified Quality Systems: Global Standard Operating Procedures (SOPs) and Quality Assurance (QA) systems ensure consistency in data, processes, and compliance.
Flexible and Scalable Capacity: Our facilities are designed to meet evolving client needs—from feasibility studies to commercial-scale batches.
Although our reach is global, our focus is personal. At every MedPharm location, you’ll find a team that is dedicated to your success and a facility built to advance your product.
21,000 sqft R&D and Clinical Supply Facility based in Guildford, Surrey, United Kingdom
100,000 soft Commercial Manufacturing and US Clinical Supply Facility located in Durham, NC