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Ethical & Robust Research during a Pandemic: HOW?

11/05/20
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Ethical & Robust Research during a Pandemic: HOW?

Research is a sprint during a pandemic.  How do you produce ethical and high quality research when you're racing to collect sensitive data and working with large teams?  What should the IRB/REC be looking for during pandemic protocol reviews? How does a pandemic impact informed consent? Find out the answers to these questions and more during our 1hr webinar: https://www.youtube.com/watch?v=GUHcwPqpp2s
 

Who should register?

Healthcare professionals who wish to be part of a unique network, providing access to up-to-date, accurate and validated information about clinical research.

Investigators and study staff who wish to be part of a unique network, in order to stay abreast of clinical trials taking place in Luxembourg and who are willing to further develop their competencies.