GC Pharma gets CRL from USFDA for ALYGLO
The FDA issues a complete response letter to indicate that the review cycle for an application is complete but the application cannot be approved in its current form.
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Yongin - GC Pharma today announced that it has received a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) in response to its Biologics License Application (BLA) for 'ALYGLO (Immune Globulin Intravenous (Human), 10% Liquid)'. The FDA issues a CRL to indicate that the review cycle for an application is complete but the application cannot be approved in its current form.
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