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Fulfills EMA GMP manufacturing and declaration to support clients intending to export gene therapy products for clinical programs in Europe.
April 24, 2023
By: Anthony Vecchione
Forge Biologics, a manufacturer of genetic medicines, announced that its manufacturing facility has successfully completed the audits necessary and received QP declaration for its gene therapy manufacturing facility, thereby fulfilling the EU Good Manufacturing Practices (GMP) requirement to manufacture investigational medicinal products and allowing Forge to support European-based clinical trials. “QP declaration enhances Forge’s position as a leading global AAV manufacturer able to support ...
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