Galderma announces progress with relabotulinumtoxinA regulatory submissions

Galderma

2 October 2023 - Galderma receives FDA complete response letter with comments isolated to Chemistry, Manufacturing, and Controls items.

Galderma announced today updates related to the regulatory progress of its pending biologics license application for relabotulinumtoxinA (QM-1114) to the US FDA.

Read Galderma press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , Dossier