From lab to trial sites - the right product in the right place at the right time in the right condition
Site-to-site connectivity – coupled with storage, shipment, and tracking resources – gives us the ability to provide seamless supply chain management. From our warehouses to your investigational sites around the globe, we make sure the correct product gets to the right place on time. Our facilities, extensive service portfolio, and professional project management distinguish us as a leader in clinical supply services. We’re fully integrated from the laboratory to the production facility to the warehouse, and our sites and systems work together to ensure fast turnaround.
Catalent Benefits
- International presence, experience, and scale with facilities in the US, UK, Germany, and Singapore
- Over 60 audited depots on 6 continents serving 80+ countries
- Cold-chain distribution management including refrigerated and frozen shipments featuring:
- 1,000,000+ cft of controlled room temperature (CRT) space
- 250,000+ cft of refrigerated space
- 21,000+ cft of frozen space
- Global distribution and tracking with experience in pharmaceutical shipping to over 75 countries
- In-depth knowledge of worldwide regulatory and import/export guidelines with:
- 25,000+ cft DEA approved vault space
- 15,000+ cft DEA approved cage space
- Return-drug reconciliation and management
Catalent Capabilities
Our material and logistics management capabilities include:
- cGMP warehousing and high-capacity storage
- cGMP warehousing and high-capacity storage
- Storage and handling of DEA-registered Schedule II - V products
- Cold-chain inventory management including refrigerated and frozen capabilities
- Customized inventory management systems
- Seamless scale-up and technology transfer
- 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
- Return-drug reconciliation and management
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, US
- Allendale, New Jersey, USA
- Kansas City, Missouri, USA
- Bolton, England
- Bathgate, Scotland
- Deeside, Wales
- Schorndorf, Germany
- Singapore