about
An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethicsTesting for sexually transmitted infections in a population-based sexual health survey: development of an acceptable ethical approachThe Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.Public preferences about secondary uses of electronic health information.An ethical hierarchy for decision making during medical emergencies.When is it rational to participate in a clinical trial? A game theory approach incorporating trust, regret and guiltInclusion of residual tissue in biobanks: opt-in or opt-out?Recruiting terminally ill patients into non-therapeutic oncology studies: views of health professionals.Principles of human subjects protections applied in an opt-out, de-identified biobank.Clinical research and medical care: towards effective and complete integrationSubversive subjects: rule-breaking and deception in clinical trials.Privacy revisited? Old ideals, new realities, and their impact on biobank regimesIntroduction: public health genomics-anthropological interventions in the quest for molecular medicineThe importance of purpose: moving beyond consent in the societal use of personal health information.Harms, benefits, and the nature of interventions in pragmatic clinical trials.Viewing research participation as a moral obligation: in whose interests?Increasing enrollment in drug trials: the need for greater transparency about the social value of research in recruitment effortsVoluntary consent: why a value-neutral concept won't workParticipants' responsibilities in clinical research.The Bio-PIN: a concept to improve biobanking.Efficient design of clinical trials and epidemiological research: is it possible?When clinical care is like research: the need for review and consent.Can research and care be ethically integrated?Exploring participant experiences of research after traumatic brain injury.Does consent bias research?Recruitment practices and the politics of inclusion in cancer clinical trials.Why do people participate in epidemiological research?Whatever Happened to Human Experimentation?Ethical justifications for access to unapproved medical interventions: an argument for (limited) patient obligations.Personal knowledge and study participation.Making the transition to a learning health care system. Commentary.Non-completion and informed consent.Proceedings of the Christiana Care Health System Value Institute Value Symposium.Using Default Options and Other Nudges to Improve Critical Care.Is there a duty to participate in digital epidemiology?Where Did Informed Consent for Research Come From?Encouraging Participation And Transparency In Biobank Research
P2860
Q28283192-30A7D71D-103C-4371-9C3F-613F8C7E620EQ28729270-20084882-D6FE-4E01-ADEA-CE31B5213C5BQ30957260-FAAC0C98-A4DF-4C7A-B790-BAF64180FDA6Q33852144-7BE509B0-8CC1-4995-B2E0-E3A465B0D849Q33872552-41FDA51B-905C-4D66-AB00-7FAC5066FD60Q34314845-EC220710-CD0F-426D-BD4D-B56C4D98654DQ34382331-6230E1A9-F2C2-40D2-B58B-D9D08E4C909DQ34502444-DA179E82-6292-45AF-B313-D529461C7034Q34788719-668ED2F9-CE50-416C-BED2-CD2364B6DC98Q35068463-833E2CCB-259B-45A3-9E55-C9D80ACB8362Q35085835-465BCA09-5857-439E-BC6F-66A6E9C02285Q35556197-F086CE3F-073C-476E-B41B-77961B519A1DQ35601513-C15DA972-C22B-4F3B-82C5-D8BA04F808D9Q36069559-EC6D3B24-DDE1-44FD-A094-E9F525BF841AQ36117803-4F27B00D-42A9-4703-B522-B1CB9CE3F0B7Q36377696-41A60938-6FD1-42F3-9417-5A8F89DEE9DDQ37059463-DCC0E5C0-E0C0-4092-BB49-6F0ED7392AB4Q37564280-CEE074AF-C7BA-4C0D-9242-5F0529D749F5Q37654584-52247427-EE31-49A2-89D3-3D93B2842C6FQ37853837-FE3CC2CC-7FE3-4EBF-B39A-27EA93044FADQ38817527-E1E50F4E-505D-46FB-88DC-4878F2BFD0D5Q38836490-1F3FACC0-7718-45D0-A77D-3F0AAA07438AQ39717107-EABAB22C-FBD7-4E60-8C8B-B673AF0D31BAQ43617297-75DDC4FF-B640-44B0-831C-162A804081A7Q45627963-65A7874D-38E0-40BA-BB52-DE90ABDFDC0EQ46034034-605DB8B6-7B2F-42E1-8774-11CCD8E47A66Q47677821-D117D8B5-A7FD-4F9A-8149-DD74163816E5Q47885638-292D127C-54E5-48C4-8907-A90F25A1690AQ48062346-1496DA5E-299E-4E23-82F4-6F885296643EQ48221240-8814FB59-E092-4FBE-85E3-4EDAE36E1452Q48292570-F9DE98D2-963D-4518-A49E-A2E937CAC228Q48306612-C90D2B5E-6D3E-40E1-B8F5-13E5169B29FAQ50870845-DA7B816B-87ED-46A5-81F6-CC1975C7B293Q53448773-6198637B-0B7E-4073-8CA4-964A48D8F6D8Q54959919-8A5B5BA3-99B3-446B-9D8B-945116F2D81BQ56568771-517AFCA6-1869-4EC1-93C9-4236C32EE3E7Q57172257-A9163EAE-AD51-4FB5-B746-8604B922CDC7
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The obligation to participate in biomedical research.
@en
The obligation to participate in biomedical research.
@nl
type
label
The obligation to participate in biomedical research.
@en
The obligation to participate in biomedical research.
@nl
prefLabel
The obligation to participate in biomedical research.
@en
The obligation to participate in biomedical research.
@nl
P2860
P356
P1476
The obligation to participate in biomedical research.
@en
P2093
G Owen Schaefer
P2860
P356
10.1001/JAMA.2009.931
P407
P577
2009-07-01T00:00:00Z