La publicación de una nueva versión de la Declaración de Helsinki es una excelente oportunidad para repensar este problema. Según mi interpretación, la . La Asociación Médica Mundial (AMM) ha promulgado la Declaración de Helsinki como una propuesta de principios éticos para investigación.
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Ver especialmente Autor b. NRESop.
Continuing navigation will be considered as acceptance of this use. All medical research involving human subjects must be preceded by careful assessment of predictable risks and burdens to the individuals and groups involved in the research in comparison with foreseeable benefits to them and to other individuals or groups affected by the condition under investigation.
This information must also be disclosed to participants during the informed consent process”. Subscribe to our Newsletter.
When the risks are found to outweigh the potential benefits or when there is conclusive proof of definitive outcomes, physicians must assess whether to decclaracion, modify or immediately stop the study. Unproven Interventions in Clinical Practice From Monday to Friday from 9 a.
Declaración de Helsinki by Pamela Dorantes on Prezi
Research on animals and current UGC guidelines on animal Subscriber If you already have your login data, please click here. The risks must be continuously monitored, assessed and documented by the researcher. This information must also be disclosed to participants during the informed consent process.
This paper presents a framework of ethical considerations regarding research on human beings, to outline a number of proposals and helsinoi on the Declaration of Helsinki Articles 2, 15, 19, 23, 32, 33, Reports of research not in accordance with the principles of this Declaration should not be accepted for publication.
There may be exceptional situations where consent would be impossible or impracticable to obtain for such research.
WMA Declaration of Helsinki – Ethical Principles for Medical Research Involving Human Subjects
According to my interpretation, the Declaration of Helsinki identifies two different types of post-trial obligations, namely, 1 obligations of access to health care and 2 the obligations of access to information.
Sobre el requisito de respuesta adecuada, respuesta adecuada [responsiveness] ver London, A. Consent to remain in the research must be obtained as soon as possible from the subject or a legally authorised representative. Princeton University Press; Autor It is the duty of physicians who are involved in medical research dee protect the life, health, dignity, integrity, right to self-determination, privacy, and confidentiality of personal information of research subjects.
Oxford University Press; Macklin, R.
Vulnerable Groups and Individuals At the conclusion of the study, every patient entered into the study should be assured of access to the best proven prophylactic, diagnostic and therapeutic methods identified by the study”.
Some groups and individuals are particularly vulnerable and may have an increased likelihood of being wronged or decclaracion incurring additional harm. The Declaration of Helsinki should be a mandatory, rather than optative, undertaking to comply, included in all the Consent Letters for participation in research trials by any human being.
The World Medical Association WMA has developed the Declaration of Helsinki as a statement of ethical principles for medical research involving human subjects, including research on se human material and data. This item has received.
Groups that are underrepresented in medical research should be provided appropriate access to participation in research. The welfare of animals used for research must be respected. It must take into consideration the hdlsinki and regulations of the country or countries in which the research is to be performed as well as applicable international norms and standards but these must not se allowed to reduce or eliminate any of the protections for research subjects set forth in this Declaration.
The ethics of clinical research, Jennifer S.