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The FDA decision provides Recipharm with a platform on which to build out its manufacturing capabilities for new modalities in the biologics space.
May 2, 2023
By: Anthony Vecchione
Recipharm, a global contract development and manufacturing organization (CDMO), announced that its subsidiary, GenIbet Biopharmaceuticals, has received U.S. FDA approval as a manufacturing site of VOWST, a breakthrough orally administered fecal microbiota product for the prevention of clostridioides difficile recurrent infection (CDI) in adults following antibacterial treatment for recurrent CDI. Recipharm will manufacture VOWST at its GenIbet site in Oeiras, Portugal on behalf of Seres Thera...
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