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Kirsten Van Garsse, Authorized Representative Director & Regulatory Affairs Manager

Recent Posts

New EMA FAQ on the Development and Assessment of Medicinal Products Involving Companion Diagnostics (CDx)w EMA FAQ on medicinal products development and assessment involving a CDx

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Events calendar

Industry
Service

enero

28.01 - 29.01

Clinical

OCT Medical Devices Europe 2025

Munich, Germany

febrero

02.02 - 06.02

Regulatory Affairs

Medlab Middle East 2025

Dubai, United Arab Emirates

marzo

11.03 - 12.03

Regulatory Affairs

RAPS Global Regulatory Strategy Conference 2025

Baltimore, Maryland, USA

mayo

13.05 - 16.05

Regulatory Affairs

RAPS Euro Convergence 2025

Brussels, Belgium
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