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EU Accelerated Assessment Tracker

 
• By Maureen Kenny

Sanofi failed in its attempt to have its EU marketing authorization application for avalglucosidase alfa fast-tracked through the centralized review process at the European Medicines Agency. This and other developments relating to the agency's accelerated assessment mechanism are logged in this latest update to the Pink Sheet's EU accelerated assessment tracker.

The tracker below provides information on accelerated assessment requests for planned marketing authorization applications (MAAs) that have come before the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP).

This latest update reflects Sanofi's failure to secure accelerated assessment for avalglucosidase alfa. Also see "Sanofi Files New...

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