Patients would benefit from simplified ethical review and consent procedure

scientific article published on 21 March 2013

Patients would benefit from simplified ethical review and consent procedure is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/S1470-2045(13)70129-3
P698PubMed publication ID23522924

P50authorRuth F. ChadwickQ62607857
Joakim DillnerQ62918677
P2093author name stringGert Jan van Ommen
Mats G Hansson
P2860cites workGene expression profiling predicts clinical outcome of breast cancerQ27860732
A gene-expression signature as a predictor of survival in breast cancerQ27860945
Should donors be allowed to give broad consent to future biobank research?Q36410751
One-time general consent for research on biological samplesQ36412166
Serologically diagnosed infection with human papillomavirus type 16 and risk for subsequent development of cervical carcinoma: nested case-control studyQ36597321
Viewpoint: why our conceptions of research and practice may not serve the best interest of patients and subjectsQ37853640
Type-specific persistence of human papillomavirus DNA before the development of invasive cervical cancerQ40788937
P433issue6
P921main subjectmedical ethicsQ237151
informed consentQ764527
research ethicsQ1132684
ethical reviewQ56515249
ethical analysisQ98139384
ethics review processQ107087694
P304page(s)451-453
P577publication date2013-03-21
P1433published inLancet Oncology CommissionQ13747613
P1476titlePatients would benefit from simplified ethical review and consent procedure
P478volume14

Reverse relations

cites work (P2860)
Q28658438A human rights approach to an international code of conduct for genomic and clinical data sharing
Q37690269An ethics safe harbor for international genomics research?
Q28636560BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres
Q45951421Natural History, Trial Readiness and Gene Discovery: Advances in Patient Registries for Neuromuscular Disease.
Q34011881RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research
Q24658614Rare disease research: Breaking the privacy barrier
Q37147743Representing life as opposed to being: the bio-objectification process of the HeLa cells and its relation to personalized medicine
Q27303838Research ethics committees in the regulation of clinical research: comparison of Finland to England, Canada, and the United States.
Q47238107The Global in Global Health is Not a Given
Q36224508The ethics of withdrawal: the case of follow-up from first-in-human clinical trials

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