Details
| Original language | English |
|---|---|
| Title of host publication | IEEE 12th International Conference on BioInformatics and BioEngineering, BIBE 2012 |
| Pages | 638-643 |
| Number of pages | 6 |
| ISBN (electronic) | 978-1-4673-4358-9 |
| Publication status | Published - 2012 |
| Event | 12th IEEE International Conference on BioInformatics and BioEngineering, BIBE 2012 - Larnaca, Cyprus Duration: 11 Nov 2012 → 13 Nov 2012 Conference number: 12 |
Publication series
| Name | IEEE 12th International Conference on BioInformatics and BioEngineering, BIBE 2012 |
|---|
Abstract
A general overview of the legal requirements for consent in health in European Union is presented and a comparison between three different usage of consent is being offered: consent for care; consent for clinical trial participation and consent for data processing. On a second stage a practical example of the strengths and weaknesses of the European concept of informed consent, the research project Linked2Safety is presented. Particular attention is being paid to the involved patients in the project, the different types of consent and the phases of the project as well as the data within the project.
Keywords
- clinical tirals, European Union framework, Infromed consent, patients, sensitive data
ASJC Scopus subject areas
- Chemical Engineering(all)
- Bioengineering
- Engineering(all)
- Biomedical Engineering
Cite this
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IEEE 12th International Conference on BioInformatics and BioEngineering, BIBE 2012. 2012. p. 638-643 6399776 (IEEE 12th International Conference on BioInformatics and BioEngineering, BIBE 2012).
Research output: Chapter in book/report/conference proceeding › Conference contribution › Research › peer review
}
TY - GEN
T1 - Strengths and weaknesses of the European concept of informed consent
T2 - 12th IEEE International Conference on BioInformatics and BioEngineering, BIBE 2012
AU - Forgó, Nikolaus
AU - Góralczyk, Magdalena
AU - Von Rex, Constantin Graf
N1 - Conference code: 12
PY - 2012
Y1 - 2012
N2 - A general overview of the legal requirements for consent in health in European Union is presented and a comparison between three different usage of consent is being offered: consent for care; consent for clinical trial participation and consent for data processing. On a second stage a practical example of the strengths and weaknesses of the European concept of informed consent, the research project Linked2Safety is presented. Particular attention is being paid to the involved patients in the project, the different types of consent and the phases of the project as well as the data within the project.
AB - A general overview of the legal requirements for consent in health in European Union is presented and a comparison between three different usage of consent is being offered: consent for care; consent for clinical trial participation and consent for data processing. On a second stage a practical example of the strengths and weaknesses of the European concept of informed consent, the research project Linked2Safety is presented. Particular attention is being paid to the involved patients in the project, the different types of consent and the phases of the project as well as the data within the project.
KW - clinical tirals
KW - European Union framework
KW - Infromed consent
KW - patients
KW - sensitive data
UR - http://www.scopus.com/inward/record.url?scp=84872874926&partnerID=8YFLogxK
U2 - 10.1109/BIBE.2012.6399776
DO - 10.1109/BIBE.2012.6399776
M3 - Conference contribution
AN - SCOPUS:84872874926
SN - 978-1-4673-4357-2
T3 - IEEE 12th International Conference on BioInformatics and BioEngineering, BIBE 2012
SP - 638
EP - 643
BT - IEEE 12th International Conference on BioInformatics and BioEngineering, BIBE 2012
Y2 - 11 November 2012 through 13 November 2012
ER -