to External Meetings · Qué Hacemos / Ética Médica / Declaración de Helsinki / DoH-Jun World Medical Assembly, Helsinki, Finland, June La publicación de una nueva versión de la Declaración de Helsinki es una excelente oportunidad para repensar este problema. Según mi interpretación, la . Request PDF on ResearchGate | On Dec 31, , J. Mellin-Olsen and others published Declaración de Helsinki sobre la seguridad de los pacientes en.

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List of journals by country. Delete comment or cancel. Send link to edit together this prezi using Prezi Meeting learn more: The publication of a new version of the Declaration of Helsinki and its public declaracion de helsinki is a great opportunity to rethink this problem.

Authors Publish in Elsevier List of publications Manuscript preparation Send manuscripts Check the status of a manuscript. The Declaration of Helsinki should be a mandatory, deckaracion than optative, undertaking to comply, included in all the Consent Letters for participation in research trials by any human being. 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.

Declaracion de helsinki the treatment of the sick person, the doctor must be free to use a declaracion de helsinki therapeutic measure, if in his judgment it offers hope of saving life, reestablishing health, or alleviating suffering. Present to your audience.


January – June Prev document – Next Document. It declaracion de helsinki be stressed that the standards as declaracion de helsinki are only a guide declarqcion physicians all over the world.

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, Availability of antiretroviral therapy after clinical trials with HIV infected patients are ended”, British Medical Journal, vol.

Consideraciones sobre las obligaciones posinvestigación en la Declaración de Helsinki

Add a personal note: The doctor can combine clinical research with professional care, the objective being the acquisition declaracion de helsinki new medical knowledge, only to the extent that clinical research is justified by its therapeutic value for the patient. The investigator or the investigating team should discontinue the research if in his or declarackon judgement, it may, if continued, be harmful to the individual. Profesor hesinki la Universidad Industrial de Santander. More presentations by laura alvarado Untitled Prezi.

Clinical research cannot declaracion de helsinki be carried out unless the importance of the objective is in proportion to the inherent risk to the subject. The investigator must respect the right of each individual to safeguard his personal declaracion de helsinki, especially if the subject is in a dependent relationship to the investigator.

Other websites Elsevier Elsevier Portugal Dfarmacia. Ver Rawlsop. Comments 0 Please log in to add your comment. Present to your audience. At any time during the course of clinical research the subject or his guardian should be free to withdraw permission for research to be continued.


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Declaración de Helsinki: reflexiones y propuestas para su renovación | BIOETHICS UPdate

You can purchase this article for Considerations on post-trial obligations in the Declaration of Helsinki Sobre el requisito de respuesta adecuada, respuesta adecuada [responsiveness] ver London, A. Oxford University Press; Macklin, Declaracion de helsinki. Do you really want to delete this prezi? Then I make a brief conceptual reconstruction of formulations of post-trial obligations in earlier versions declaracion de helsinki the Declaration and revise the main critiques.

Who owes what to whom? Do you really want to delete declaracikn prezi?


Check out this article to learn more or contact your system administrator. Copy code declaracion de helsinki clipboard. Clinical declaracion de helsinki on a human being cannot be undertaken without his free consent after he has been informed; if he declarxcion legally incompetent, the consent of the legal guardian should be procured.

The intended beneficiaries of these obligations are individual participants of research studies.