With unwavering dedication to serving clinical research and patients around the world, we are powered by people with an exceptional commitment to delivering end-to-end, high quality global clinical supply chain services.
Whether you need primary or secondary packaging of your clinical drug, storage, distribution, logistics, cold chain management, or comparator and ancillary sourcing, our global team can meet the needs of every trial regardless of size, phase or therapeutic area. We also offer import/export services, including Importer of Record (IOR) capability in more than 25 countries to date, and best-in-class direct-to-patient services.
We are committed to delivering the highest possible value while ensuring adherence to the highest level of quality, performance, reliability and sustainability standards.
We offer the industry’s largest network of fully owned cGMP facilities strategically located around the world to support the conduct of clinical trials.
Our 27 purpose-built GMP/GDP compliant facilities, supported by over 38 partner depots—located across five continents—provide the global presence, information systems and quality standards to provide clients the flexibility, access and assurance needed for their clinical trial.
What’s more, our continued investment in cold chain storage capacity, as well as distribution capability across the network, mirrors the industry’s evolution to handle increased quantities of complex cold chain biologics across many continents.
With our global reach and local care, we can meet your unique requirements, no matter where in the world you’re conducting your trial. Contact us to learn how we can help with your next clinical trial.
Learn about primary and secondary packaging of clinical trial materials at our Horsham, UK site. This site also specializes in automated global distribution and expertise in Cold Chain Management.
Avoid derailing your clinical trial. Consider these important factors when developing your clinical supply planning strategy.