HemaCare Corporation announced that it has expanded its portfolio of GMP-compliant cellular material with the launch of the GMPrime cryopreserved leukopak. The GMP-compliant cryopreserved leukopak includes a quality assurance (QA)-reviewed Certificate of Analysis, thus adding QA review to HemaCare’s popular research use (HemaPrimeTM) cryopreserved leukopak. HemaCare’s GMPrime leukopaks are cryopreserved following a proprietary cryopreservation process and meet the requirements of the most rigorous quality standards required by regulatory agencies. GMPrime cryopreserved leukopaks extend shelf life and stability and provide researchers and cell therapy developers with the consistency needed in a cellular starting material used for the development and commercialization of next-generation cell and gene therapies. GMPrime cryopreserved leukopaks are collected within HemaCare’s FDA-registered collection center from IRB-consented donors and immediately cryopreserved onsite within Class A and B (ISO 5 and 6) cleanroom environments. HemaCare’s HemaPrime and GMPrime cryopreserved leukopaks adhere to the same stringent quality standards and are collected and processed following standardized protocols to ensure the highest achievable purity, viability, and quality thus ensuring researchers can seamlessly transition from development to clinical trials to commercialization with confidence.