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Center for Breakthrough Medicines Offers Preclinical Package for IND-enabling Activities

Aims to enable the generation of high quality material and data in under five months to move rapidly towards IND approval and GMP clinical manufacturing.

The Center for Breakthrough Medicines (CBM), a contract development, manufacturing, and testing organization (CDMO) is packaging their preclinical capabilities into an IND-enabling offering to help innovator companies manufacture high quality drug substance and drug product for preclinical studies needed for IND-enabling activities. Preclinical assessment of investigational cell and gene therapy products is a critical milestone to move programs forward while balancing limited capital allocate...

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