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Connell - O'Reilly Cell Manipulation Core
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The mission of the Cell Manipulation Core Facility is to produce safe and effective cellular components for novel therapeutic clinical research protocols. To fulfill this mission all procedures are performed according to current Good Manufacturing Practices (cGMP) for cell and tissue processing. The policies and procedures established in the facility comply with all current accreditation agency and governmental standards and regulations, ensuring the production of safe, effective components for clinical use. Cellular products processed by the CMCF are provided in the context of clinical research protocols that have been reviewed and approved by the DF/HCC Scientific Review Committee and Human Subjects Protection Committee. The CMCF is available to both clinical and laboratory investigators
at all DF/HCC institutions and will provide services to patients at all
DF/HCC affiliated hospitals. The staff of the CMCF are committed to working
with DF/HCC investigators at all levels of clinical trial development
and execution, including pre-clinical development, trial design, DF/HCC
and FDA review, data management, quality control, internal and external
audits as well as reports and publications. The Cell Manipulation Core
Facility (CMCF) has been accredited by the Foundation
for the Accreditation of Hematopoietic Cell Therapy (FAHCT) laboratory.
The CMCF is a member of the Joint Program in Transfusion Medicine. Please click here to go to the Cell Manipulation Core:
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