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
for articles/videos/studies
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.
