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Austria Center Vienna

2019年2月05日 (火) 午前 7:00 - 2019年2月07日 (木) 午後 5:00

Bruno-Kreisky-Platz 1, 1220 Vienna, Austria

DIA EUROPE 2019

Oral Poster Session 4 - Regulatory Science & Value and Access Content Hub

Learning Objective : The aim of our study was to understand the current status and trends of the Breakthrough Designation (BTD), PRIME and SAKIGAKE expedited review programs regarding number of reviews, most benefited therapy areas, drugs reviewed, profile of applicants and time to regulatory approval.

Speaker(s)

Pedro  Borga, MPHARM

An overview of the current status and trends in the Breakthrough Designation, PRIME and SAKIGAKE expedited review programs

Pedro Borga, MPHARM

Lifescience Dynamics Ltd, United Kingdom

Consultant

Camille  Metais, MSC

Early Actions granted by FDA: a review of the frequency and importance of NDA/BLA approvals in advance of DUFA action date

Camille Metais, MSC

Alexion Pharma GmbH, Switzerland

Senior Director Regulatory Affairs

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