Browse our Cell Sourcing Products and Services
Cell Processing and Isolation Solutions
Achieve your project goals faster with our cell isolation and cryopreservation expertise. Our cell sourcing capabilities include on-site collections with same-day processing, carefully optimized protocols, and rigorous QC testing to rapidly deliver pure, viable, consistent, and highly functional cellular starting material to quickly advance your project through its product development pipelines.
Let's Work Together
Targeted Donor Selection and Sourcing
Ensure consistent access to recallable donors throughout your cell therapy program. With over 40 years of experience building long-term donor relationships, HemaCare Donor Center (a Charles River company) has built a vast network of well-characterized donors that are readily available for the development of autologous and allogeneic cell-based therapies.
Learn About Donor Recruitment
Cell Cryopreservation: Advantages for Cellular Starting Material
Starting material and immune cell stability is one of the most critical factors behind the success of any immunotherapy product. Cell cryopreservation is an important tool for managing variability associated with starting material stability, locking in viability and potency, and provides researchers with reliable, on-demand cellular starting material for next-generation cell and gene therapies.
Learn About Cell Cryopreservation
Quality Standards
-
Licensure and Accreditation
Charles River complies with documented procedures governing the sourcing, handling, processing, storage, preserving, packaging, and distribution of products. Charles River is FDA registered (Blood and HCT/P) and meets all applicable GMP/GTP standards (21 CFR 210, 211, 606, 1271 and 21 CFR part 11 and part 58). Charles River also ensures that all sites including Lowell (Blood and HCT/P) and Memphis (Blood and HCT/P) are FDA-registered. Charles River maintains compliance with the State of California Laws and Regulations for production of biologics and tissue banking, meets CLIA requirements to ensure the accuracy and reliability of quality control testing and is AABB-accredited, which verifies that an appropriate quality management system and controlled collection processes are in place. In addition to the FDA, Charles River complies with European Medicines Agency (EMA) guidelines and our GMP-compliant facility is routinely audited by the FDA, State of California, and AABB.
-
Terms & Conditions
Pricing is subject to Terms and Conditions – Cell Sourcing.
-
How to Order
Please see How to Order – Cell Solutions.
10 Questions to Ask Your Apheresis Provider
The link between a consistent cell supply and successful cell therapies to learn how a large, diverse donor pool gives researchers access to project-specific physiological or demographic traits and more.
Get the Answers