Anna Chiotis' presentation at the 5th Clinical Research Day 2013
5min10
E Film den erkläert wéi klinesch Fuerschung funktionéiert. watch...
10min07
Introduction of the 5th Clinical Research Day 2013 watch...
24min44
Nikolai Goncharenkos' and Serge Haans' presentations at the 5th Clinical Research Day 2013 watch...
22min18
Anna Chiotis' presentation at the 5th Clinical Research Day 2013 watch...
56min00
Panel Discussion at the 5th Clinical Research Day 2013 watch...
17min38
Presentation by Dr Monique Aubart and Luisa von Zedlitz at the 5th Clinical Research Day 2013 watch...
22min41
Presentation at the 5th Clinical Research Day 2013 watch...
15min45
Dr Zügels' presentation at the 5th Clinical Research Day 2013 watch...
12min55
Manon Gantenbeins' presentation at the 5th Clinical Research Day 2013 watch...
51min30
Ingrid Klingmanns' presentation at the 5th Clinical Research Day 2013 watch...
25m 18s
Dr. Michael Carome, former OHRP Associate Director of Regulatory Affairs, is interviewed and discusses the criteria for determining if, in the context of human subjects research, an experience, incident, or outcome is an unanticipated problem involving risk to subjects or others, as described in the HHS regulations at 45 CFR part 46. watch...
28m 13s
This video presentation on the additional protections for certain vulnerable subjects, including pregnant women, children, and prisoners starts out at the end of a panel presentation on the additional protections afforded to vulnerable populations described in the subparts B, C, and D or the HHS regulations at 45 CFR part 46. watch...
18m 39s
In this video, all of the characters are fictional.In the first scene an investigator meets with the IRB Chair to discuss issues for obtaining informed consent from potential subjects with schizophrenia before protocol submission to IRB. In the second scene, Dr. Presley obtains appropriate informed consent from a potential subject, Mr. Smith, who has the capacity to consent. watch...
2m 16s
This video shows the Clinical and Epidemiological Centre within CRP-Santé and its role in promoting clinical research in Luxembourg. watch...
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.
