EU Health Authorities Scientific and Regulatory Advice

NEW OFFERING! The course is built up as a dialogue between industry and regulator perspective and will teach you what authorities pay attention to, what inquiries they make and what they expect to hear from sponsors.

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GROUP EXERCISE TO REFLECT ON THE TOPICS COVERED IN SESSION 1

Session Chair(s)

Birka Lehmann, MD

Senior Expert Drug Regulatory Affairs

Birka Lehmann, Germany

Trine B. Moulvad, MSc

Global RA, Medical Documentation and R&D QA

Lundbeck, Denmark

Speaker(s)

GROUP EXERCISE TO REFLECT ON THE TOPICS COVERED IN SESSION 1

Trine B. Moulvad, MSc

Lundbeck, Denmark

Global RA, Medical Documentation and R&D QA

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EU Health Authorities Scientific and Regulatory Advice

GROUP EXERCISE TO REFLECT ON THE TOPICS COVERED IN SESSION 1

Session Chair(s)

Birka Lehmann, MD

Trine B. Moulvad, MSc

Speaker(s)

GROUP EXERCISE TO REFLECT ON THE TOPICS COVERED IN SESSION 1

Be informed and stay engaged.