Workshop - Beyond the Fine Print: Rethinking Informed Consent for European Drug Trials

start with data from a current research project

overview of the ethical and regulatory framework for informed consent

questionnaire and hands-on exercises with sample consent forms

focus on risk communication

role-play and group work to integrate different stakeholder perspectives and co-create recommendations

pharmakologisch tätige ÄrztInnen und WissenschafterInnen

Überregional

Prof. Dr.med.univ. ROMUALD BELLMANN
E-Mail: romuald.bellmann@i-med.ac.at
Telefon: +43 512 504 81389

Dr. EVA MARIA ZEBEDIN-BRANDL
E-Mail: eva-maria.zebedin@meduniwien.ac.at
Telefon: +43 1 40160-31320

Dr. EVA MARIA ZEBEDIN-BRANDL

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