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gesine

Seminar Title

 

Seminar M4 – Design for safety in drug development

Affiliation

vfa.Research-based Pharmaceutical Companies

Country

Germany

1. Current Status, Position

Senior Manager responsible for topics related to Regulatory Affairs/Quality/Environment.

2. Education

Dr. Gesine Bejeuhr started her career as inspector (for pharmacies, hospitals, GMP) and scientific administrator in Germany (including a one-year-secondment to the European Medicines Agency’s inspections sector; focus: mutual recognition agreement between the EU and Japan).
Prior to joining vfa in 2008 she was responsible for Regulatory Affairs & Safety Intelligence at Grunenthal, Germany.
She dealt with the cross-functional implementation of new legislative requirements such as e.g. the EU Paediatric Regulation.

3. Research Area

Coordinating several expert groups in the area of Drug Regulatory Affairs, Quality and Environment with a focus on patient and HCP-friendly product information.

Conflict of interest: Employee for Research-based pharmaceutical Industry association.

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Deadline extended to July 15th

Problems caused by shortages are serious, threaten patient care and require urgent action.

Help us provide an overview of the scale of the problem, as well as insights into the impact on overall patient care.

Our aim is to investigate the causes of medicine and medical device shortages in the hospital setting,  while also gathering effective solutions and best practices implemented at local, regional, and national levels.

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Join us in Prague for the 2nd edition of BOOST!

Secure your spot in the Movement for Shortage-Free World

BOOST is where visionaries, innovators, and healthcare leaders come together to tackle one of the biggest challenges in hospital pharmacy—medicine shortages.