Webinar | June 7, 2023

Meeting GMP Requirements For Allogeneic Cell Therapies: Regulations, Cleanroom, And Data Integrity

Learn why failure to include at least some elements of GMP in your cell line design and development process could make it more difficult to get the data required for future IND or BLAs. This overview discusses regulations alongside the equipment and supplies that should be evaluated for GMP compliance as part of your CLD workflow design stage.

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