The Scientific Affairs group establishes and maintains continued financial support from our vendor partners and government contracts to conduct research studies and clinical trials focused on current and emerging transfusion-transmitted infectious disease agents. Our group has access to normal (infectious disease marker-negative) and marker-reactive blood samples representing a broad and geographically diverse population of the US, which can be utilized for potential new studies. Data supporting the characterization of our materials are available upon request. Data derived from these studies are used to support blood screening assay and pathogen reduction technology development, to affect policy decision making with respect to donor and recipient safety, and to recommend appropriate interventions as needed.
The Transfusion Innovation groups in Rockville, MD and Norfolk, VA provide testing and performance assessment services (Test and Evaluation) for manufacturers and commercial organizations in the product development lifecycle of new and modified medical devices, technologies and processes for the collection, manufacture, storage, and testing of blood and blood products according to industry standards and in support of FDA licensure.
In addition, the Norfolk, VA group assists companies with licensing studies (including radiolabeling in vivo procedures) for new blood products, new storage containers, platelet and red cell additive solutions, leukoreduction, irradiation, frozen blood, cell processing and washing, anaerobic storage and pathogen inactivation.