Clinical Supply Services Overview

Integrated Pharma Resources and Superior Project Management Services When and Where You Need Them

With 9 facilities in the US, EU, and Asia/Pacific region, and more than 60 depots covering 6 continents, Catalent Clinical Supply Services has a robust network built around the most complete integrated service offerings for pharmaceuticals in clinical trial phases I-IV. We provide reliable service and deeper expertise in global supply chain and project management that will speed your drug to clinic.

At Catalent we recognize that in today’s challenging clinical environment, every project is different. Changes occur frequently during the development phase that require unique solutions and a high degree of flexibility. Catalent’s expert teams offer creative solutions and provides the flexibility necessary for your clinical trial success.

Catalent Benefits

• Industry-leading experience and resources
  • Over 25 years in the clinical supplies industry
  • 4,500+ Clinical Trials supported
  • Serving the top 25 Pharma and 300+ virtual and small companies
  • 99% on-time delivery record built on 150,000 shipments a year to 80+ Countries
  • A proven track record in worldwide logistics management, project management, and regulatory affairs
• Global infrastructure 
  • Our facilities in the U.S., U.K., Germany, and Singapore are fully inspected and certified by the appropriate U.S. and European regulatory agencies, allowing us to support global studies from any site and feature:
  • 100+ primary and secondary packaging suites
  • 1,400,000+ cubic feet of controlled temperature space
  • 800+ DEA Sch, I-V pallet spaces
• Unmatched capabilities 
  • From direct comparator sourcing to manufacturing and packaging for all dosage forms to proprietary compliance packaging solutions to help you improve study outcomes

Catalent Capabilities

Catalent is a leader in providing you with the full spectrum of support including:

• Seamless scale-up and technology transfer
• Superior end to end Cold Chain capabilities
• Full DEA Schedule I-V capabilities; including manufacturing, import/export, and storage
• Access to a comprehensive continuum of services ranging from discovery support to launch
• Coordinated project management from the clinical stage to commercialization
• Full regulatory affairs assistance, including regulatory agency liaison, preparation of expert reports, clinical trial applications, and compilation of dossiers

Facilities

With uniform systems and facilities in the US, UK, Germany and Singapore - and an extended network of over 60 audited depots - our capacity enables us to adapt to and handle all your international compliance and distribution needs, ultimately reducing your turnaround time.

• Philadelphia, Pennsylvania, USA
• Mount Laurel, New Jersey, USA
• Allendale, New Jersey, USA
• Kansas City, Missouri, USA
• Bolton, England 
• Bathgate, Scotland
• Deeside, Wales
• Schorndorf, Germany
• Singapore