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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Although it may be appropriate to consult family members or community leaders, no individual capable of delaracion informed consent may be enrolled in a research study unless he or she freely agrees.

The responsibility for the protection of research subjects must always rest with the physician or other health care professionals and never with the research subjects, helsinnki though they have given consent. In such situations the research may be done only after consideration and approval of a research ethics committee.

Declaración de Helsinki, principios y valores bioéticos en juego en

All vulnerable groups and individuals should receive specifically considered protection. Scientific Requirements and Research Protocols Said Declaration is a helsjnki paper which has been widely accepted world-wide, and as such, deserves constant reflection on its contents, to match the fast-paced progress made in the application of Science to the Biomedical research.

Privacy and C onfidentiality This website uses cookies to ensure you get the declaracioh experience on our website. The researcher must provide monitoring information to the committee, especially information about any serious adverse events.

This paper presents a framework of ethical considerations regarding research on human beings, to outline a number of proposals and argumentations on the Declaration of Helsinki Articles 2, 15, 19, 23, 32, 33, Medical research should be conducted in a manner that minimises possible harm to the environment.

Participation by individuals capable of giving informed consent as subjects in medical research must be voluntary.


Sources of funding, institutional affiliations and conflicts of interest must be declared in the publication. Philosopher’s Index See more Follow us: 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. Medical research involving human subjects must conform to generally accepted scientific principles, be based on a thorough knowledge of the scientific literature, other relevant sources of information, and adequate laboratory and, as appropriate, animal experimentation.

The potential subject must be informed of the right to refuse to participate in the study or to withdraw consent to participate at any time without reprisal. Legal, ethical and practical issuesworkshop, http: The intended beneficiaries of these obligations are individual participants of research studies.

The ethics of clinical research, Jennifer S. Medical research involving human subjects must be conducted only by individuals with the appropriate ethics and scientific education, training and qualifications. Ezekiel Emanuel, fue jefe del Departamento desde hastay fue sucedido por Christine Grady quien es la actual jefa del Departamento.

Declaración de Helsinki by Pamela Dorantes on Prezi

Who owes what to whom? Se continuar a navegar, consideramos que aceita o seu uso.

Research Registration and Publication and Dissemination of Results In medical research involving human subjects capable of giving informed consent, each potential subject must be adequately informed of the aims, methods, sources of funding, any possible conflicts of interest, institutional affiliations of the researcher, the anticipated benefits and potential risks of the study and the discomfort it may entail, post-study provisions and any other relevant aspects of the study.

This information must also be disclosed to participants during the informed consent process”. Medical research involving human subjects may only declaracioon conducted if the importance of the objective outweighs the risks and burdens to the research subjects.

If the consent cannot be expressed in writing, the non-written consent must be formally documented and witnessed. Every research study involving human subjects must be registered in a publicly accessible database before recruitment of the first subject.


WMA Declaration of Helsinki – Ethical Principles for Medical Research Involving Human Subjects

Consistent with the mandate of the WMA, the Declaration is addressed primarily to physicians. The design and performance of each research study involving human subjects must be clearly described and justified in a research protocol. Bioethics has also shown a considerable variety of ethical doctrines, schools, inspirations that has often led to irreconcilable proposals for the solution of concrete problems, and has introduced a polemical vein in the debates.

You can change the settings or obtain more information by clicking here. Considerations on post-trial obligations in the Declaration of Helsinki decoaracion In such situations the informed consent must be sought by an appropriately qualified individual who is completely independent of this relationship.

Where for compelling and scientifically sound methodological reasons the use of any intervention less effective than the best proven one, the use of placebo, or no intervention is necessary to determine the efficacy or safety of an intervention.

Risks, Burdens and Benefits The scope of this journal will correspond to the wide horizon of themes helsini problems that are now included in the domain of bioethics, and special stress will be laid on the interdisciplinary methodology required for a profitable work in dd field.

From Monday to Friday from 9 a. 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 identifiable human material and data.