Abstract
© AlphaMed Press 2016. The discovery of induced pluripotent stem cells and the ability to manufacture them using clinically compliant protocols has the potential to revolutionize the field of regenerative medicine. However, realizing this potential requires the development of processes that are reliable, reproducible, and cost-effective and that at the same time do not compromise the safety of the individuals receiving this therapy. In the present report, we discuss how cost reductions can be obtained using our experience with obtaining approval of biologic agents, autologous therapy, and the recent approval of cord blood banks.
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CITATION STYLE
Rao, M. S., & Atala, A. (2016). Developing Induced Pluripotent Stem Cell-Based Therapy for the Masses. Stem Cells Translational Medicine, 5(2), 129–131. https://doi.org/10.5966/sctm.2015-0184
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