Sourcing clinical trial ancillary supplies is much more than just procurement. It requires an understanding of the study’s design and requirements, in-depth knowledge of international regulations, and rigorous proactive planning to ensure that the most appropriate equipment and materials are purchased provided at the right time and at a competitive price.
Our Clinical Ancillary Management team has the clinical expertise and experience to understand your study’s requirements along with unparalleled access to Thermo Fisher Scientific’s vast array of laboratory and clinical products.
This superior sourcing power is combined with the distribution expertise of our Clinical Trial Services to provide a single point of support to supply and transport ancillary supplies across the globe. This seamless and coordinated process reduces the burden on both the clinical teams and the sites. Our on-the-ground personnel—strategically located around the world—offer local support for customs and import requirements, and our network of facilities provides our clients with a closed loop system for maintaining visibility and access to their ancillary supplies.
Our end-to-end services in accordance with clinical trial requirements and international regulations include:
We’re constantly monitoring the global regulatory framework in order to have a fully compliant supply chain (e.g U.S. Affordable Care Act / Sunshine Act). Through harmonizing procedures with one global quality system and fully qualifying all suppliers, we secure the supply chain and avoid substandard products.
Thermo Fisher Scientific is your best partner to integrate clinical ancillaries into your clinical supply chain. Contact us to discuss how we can help you with your clinical trial.
Clinical Trial ‘Must-Haves’ that Require Early Planning