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You are watching: Video of the Panel Discussion "Facilitating research through collaboration"

Release date: 19.12.13 Duration:  56min00

Panel Discussion at the 5th Clinical Research Day 2013

Clinical Research Videos

 
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E Film den erkläert wéi klinesch Fuerschung funktionéiert. watch...

 
Introductions by Dr Jean-Claude Schmit and the Minister of Health Mars Di Bartolomeo
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Introduction of the 5th Clinical Research Day 2013 watch...

 
The benefits of a structured collaboration in oncology research: the SOCS Study by Nikolai Goncharenko and Serge Haan
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Nikolai Goncharenkos' and Serge Haans' presentations at the 5th Clinical Research Day 2013 watch...

 
Infrastructures for excellence in clinical research by Dr Anna Chioti
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Anna Chiotis' presentation at the 5th Clinical Research Day 2013 watch...

 
Video of the Panel Discussion "Facilitating research through collaboration"
19.12.13

56min00

Panel Discussion at the 5th Clinical Research Day 2013 watch...

 
Qualcopc trial: performance in primary care in Luxembourg - Different perspectives
19.12.13

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Presentation by Dr Monique Aubart and Luisa von Zedlitz at the 5th Clinical Research Day 2013 watch...

 
The journey of translating a research idea into personalized medical care: the LCS by Dr Guy Berchem, Dr Laurent Antunes & Roxane Batutu
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Interim results of the ENHANCE study by Dr Zügel
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Dr Zügels' presentation at the 5th Clinical Research Day 2013 watch...

 
ENHANCE Study Audit by Dr Manon Gantenbein
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Good Clinical Practice: interactive presentation and quizz by Ingrid Klingmann
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Ingrid Klingmanns' presentation at the 5th Clinical Research Day 2013 watch...

 
CIEC Anniversary
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CIEC Anniversary 2013 watch...

 
Reviewing and Reporting Unanticipated Problems and Adverse Events
20.03.11

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...

 
Complex Issues with Research Involving Vulnerable Populations
20.03.11

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...

 
General Informed Consent Requirements
20.03.11

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...

 
CIEC Presentation
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2m 16s

This video shows the Clinical and Epidemiological Centre within CRP-Santé and its role in promoting clinical research in Luxembourg. watch...

 
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