How much GMP do we need to infuse contaminated HPC and DLI products?

Over the last two decades, rapid technological advances have led to the wide adoption of cell and gene therapy products for the treatment of a variety of disease states. In this study, we reviewed the literature between 2003 and 2021 to provide a summary of overarching trends associated with microbial contamination in hematopoietic stem cells (HSCs) derived from peripheral blood, bone marrow, and cord blood.

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How much GMP do we need to infuse contaminated HPC and DLI products?

Cited by 2 publications

References 3 publications

Infectious Disease Testing to Optimize Safety of Hematopoietic Stem Cell Transplant Products

Infectious Disease Testing to Optimize Safety of Hematopoietic Stem Cell Transplant Products

Sterility Testing for Hematopoietic Stem Cells

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