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Our Horsham facility provides automated global distribution and integrated biologic product capabilities. Its specialized capabilities include:
- Experienced Qualified Persons (QPs) with a deep understanding of current legislation for all aspects of clinical trial management in Europe, the US and ROW
- A Center of Excellence Learning Laboratory dedicated to off-line training of operational employees, keeping them updated on the very latest SOP procedures & best practices in the industry
- The only supplier able to offer ‘Goods for Testing Relief Service’ resulting in zero VAT and zero duty payments
- Established best practices to address Brexit scenarios, with Qualified Person (QP) cross agreements with Basel, CH and Weil am Rhein, DE facilities to allow trade flow
Benefits to Sponsors
- Long-established reputable provider in defining best practices in the industry with continued investments in capacity, capabilities and expertise
- Comprehensive service line supporting all aspects of clinical trial supply—primary & secondary packaging, labeling, regulatory support, distribution, returns and destruction
- Collaborative, flexible approach to meet client needs—new & emerging pharma & large pharma portfolio of clients, across all phases & therapeutic areas
- Track record of excellence in managing high volumes of clinical supplies
- Delivering 1,800+ primary & secondary packaging jobs and 3.4M units/kits (2018) executed at 98.3% on-time, in full
- 93,000+ shipments (2018) across 80+ countries, often to very remote locations in emerging regions, with 99.8% on-time delivery
- Flexibility to handle all types of clinical studies from Phase I to Investigator Initiated Studies (IIS), to the larger, more complex Phase II and Phase III studies
- Ability to handle compounds that are light sensitive and/or compounds with zero tolerance for Time Out of Environment (TOE), as well as handle supplies from -190°C
Download the site capabilities fact sheet to learn more about this location.