Red Blood Cells
Red blood cell units are produced from whole blood collected from subjects qualified in accordance with current regulations and requirements for donors of transfusible blood components, including screening with the Uniform Donor History Questionnaire developed by the AABB and approved by the Food and Drug Administration for screening of donors of transfusible blood components.
Selection criteria may be adjusted at the request of the customer depending on the intended use of the product and the customer’s requirements, provided that subject safety requirements are met. At the customer’s request, subjects with a history of travel or medication ingestion that would preclude them from providing a blood product suitable for transfusion may provide whole blood for production of red blood cells for non-clinical and non-injectable uses.
We also offer qualification samples on potential subjects to allow the end-user to determine suitability for targeted materials. Specific subjects may be requested for product collection. Subjects may donate as often as once every eight weeks and up to six times in any 12-month period.
Subjects are usually prescreened prior to product collection for evidence of transmissible infectious diseases with the standard panel of tests used to screen blood products for transfusion acceptability. This panel of tests is usually repeated with each collected product.
Whole blood units are usually collected into a standard blood bag system used for collection of whole blood for transfusion and containing CPDA-1 or CP2D anticoagulant. Red blood cell units are produced using centrifugation without disrupting the closed system in which the whole blood was collected. Post-production filtration through a leukocyte-reduction filter results in a product with less than 5x106 residual leukocytes in the final product. Non-leukocyte-reduced products are also available.
Depending on the intended use of the collected product, red blood cells may be produced from a whole blood unit collected into a bag system containing heparin sodium. Products collected in this manner cannot be used for clinical research.
Specific subjects may be selected from our database based on:
- Blood type
- Gender
- Ethnicity
- Human Erythrocyte Antigen genotype
Optional pre-collection qualification screening is available:
- Cell counts
- Anti-HLA Class I or Class II antibodies screen
- Recent medication usage
Optional post-collection release screening is available:
- Hematocrit
- Weight and/or volume
Packaging and Shipment
In alignment with the intended use of the product and the customer’s requirements, red blood cell units can be packaged and shipped on the date of collection for overnight delivery.
Products are packaged in a manner that ensures maintenance of a temperature between 1°C and 10°C during shipment. Continuous temperature monitoring data tracking devices are available for use at the customer’s request. |