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Virtual Event

Jun 29, 2020 8:00 AM - Jul 03, 2020 6:00 PM

(W. Europe Standard Time)

4051 Basel, Switzerland

DIA EUROPE 2020

On-Demand: Regulatory Science Hub Session

Learning Objective : To identify the main parameters to collect in a registry to be used for regulotory decision-making processes. To compare the collection of data in clinical practice versus the regulatory requirements.

Speaker(s)

Carla  Jonker, MS

Registries to be used in the regulatory decision-making process, what is minimally needed?

Carla Jonker, MS

Medicines Evaluation Board (MEB), Netherlands

Senior Regulatory Project Leader

Niels Buch Leander, PhD

The impact from EMA’s telematics strategy and SPOR program

Niels Buch Leander, PhD

NNIT, Denmark

Associate Vice President, Global Head of Regulatory Affairs

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