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Business · 05/03/2014

FDA Announces Guidance for Industry: Biologics License Applications for Minimally Manipulated, Unrelated Allogeneic Placental/Umbilical Cord Blood

The Food and Drug Administration (FDA) has released a document providing recommendations for manufacturers of cord blood banks on how to apply for a biologics license for minimally manipulated, unrelated allogeneic placental/umbilical cord blood intended for patients with hematopoietic disorders, following a finalization of the draft guidance in June 2013 and superseding a previous guidance from 2013.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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