In late January, a bill to amend the Pharmaceuticals and Medical Devices Act cleared key legislation review processes by the…
BUSINESS
European Regulators Accept Aducanumab for Review: Biogen/Eisai
Biogen and partner Eisai said on October 30 that a marketing authorization application for their investigational Alzheimer’s disease drug aducanumab has been accepted for review by the European Medicines Agency (EMA). The drug will now be reviewed by the regulator…
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