With eight 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 clinical project management that will speed your drug to market.
In today’s challenging environment, every project is different. Changes occur frequently during development that require unique, responsive solutions. With Catalent, you get that flexibility at every step—whether you’re using our preclinical services or going further into the clinical supply chain. You can rely on us for creative solutions and comprehensive clinical project management.
Benefits:
- Industry-leading experience, clinical project management and resources -
- Over 25 years in the clinical supplies industry
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5,000+ Clinical Trials supported
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Serving pharma’s top 25 plus more than 300 virtual and small companies
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99% on-time delivery record built on 150,000 shipments a year to 80+ countries
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A proven track record in preclinical services, worldwide logistics management, clinical project management, and regulatory affairs
- Global infrastructure -
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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
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100+ primary and secondary packaging suites
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1,400,000+ cubic feet of controlled temperature space
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800+ DEA Sch, I-V pallet spaces
- Unmatched capabilities -
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From direct comparator sourcing to manufacturing and packaging for all dosage forms to proprietary compliance packaging solutions to help you improve study outcomes
- Fast, accurate, and reliable storage cost estimates with Catalent WebQuote™
Features:
- A wide range of preclinical services
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Seamless scale-up and technology transfer
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Superior end to end Cold Chain capabilities
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Full DEA Schedule I-V capabilities; including manufacturing, import/export, and storage
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Access to a comprehensive continuum of services ranging from discovery support to launch
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Coordinated project management from the clinical stage to commercialization
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Full regulatory affairs assistance, including regulatory agency liaison, preparation of expert reports, clinical trial applications, and compilation of dossiers