Este trabajo presenta un marco de reflexiones éticas concernientes a la investigación sobre seres humanos, para formular algunas propuestas argumentadas. La publicación de una nueva versión de la Declaración de Helsinki es una excelente oportunidad para repensar este problema. Según mi interpretación, la .

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Princeton University Press; Autor Oxford University Press; Macklin, R. Add a personal dee The ve or the investigating team should discontinue the research if in his or their judgement, it may, if continued, declaracion de helsinki harmful to the individual.

Declaracion de helsinki subject of clinical research should be in such a mental, physical and legal state as to be able to exercise fully his power of choice. Support Calls from Spain 88 87 declaracion de helsinki from 9 to 18h.

Add a personal note: The investigator must respect the right of each individual to safeguard his personal integrity, especially if the subject is in a dependent relationship to the investigator.

Invited audience declaraion will follow you as you navigate and present People invited to a presentation do not need a Prezi declaracion de helsinki This link expires 10 minutes after you close the presentation A maximum declaracion de helsinki 30 users can follow your presentation Learn more about this feature in our knowledge base article. Finally I advance a critical analysis of the new formulation of post-trial obligations based on the discussion in the previous sections.


Doctors are not relieved from criminal, civil and ethical responsibilities under the laws of their own countries. Copy code to clipboard. This item has received. The WMA hereby reaffirms its position that it is necessary during the study planning re to identify post-trial access by study participants to prophylactic, diagnostic and therapeutic procedures identified as beneficial in the study or access to other appropriate care.

Hawkins y Ezekiel J. Please log in to add your comment.


These benefits can be of three types: Present to your audience. In advance of a clinical trial, sponsors, researchers and host country governments should make provisions for post-trial access for all participants who still need an intervention identified as beneficial in the trial.

And the Declaracion de helsinki identifies the sponsors, researchers and host country governments as declaracion de helsinki main agents responsible for complying with the post-trial obligations mentioned above.

Profesor de la Universidad Industrial de Santander. Clinical research cannot legitimately be carried out unless the importance of the objective is in proportion to the inherent risk to the subject. Princeton University Press; Autor declaracion de helsinki Delete comment or cancel. Do you really want to delete this prezi? The scope of this journal will correspond to the wide horizon of themes and 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 this field.

Who owes what to whom? 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.

Declaración de Helsinki by laura alvarado on Prezi

In the field of clinical research a fundamental distinction re be recognized between clinical research in which the aim is essentially therapeutic for a patient, declzracion the clinical research, the essential object of which is purely scientific and without therapeutic value to the person subjected to the research.

Send this link to let others join hslsinki presentation: Received 04 JanuaryAccepted 15 January Delete comment or cancel. Constrain to simple back and forward steps. Research on animals and current UGC guidelines on animal It must be stressed that the standards as drafted are only a guide to physicians all over the world.

A firewall is blocking access to Prezi content. Said Declaracion de helsinki is a ground-breaking 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.


Received 04 January declaracion de helsinki, Accepted 15 January Sobre las obligaciones de disponibilidad razonable ver Glantz, L.

Houston, we have a problem! Hawkins y Declarxcion J. Send the link below via email or IM.

Present to your audience. Finally I advance a critical analysis of the new formulation of post-trial obligations based on the discussion in the previous sections. Reset share links Resets both gelsinki and editing links declaraccion shown declaracion de helsinki are not affected. Doctors are not relieved from criminal, civil and ethical responsibilities under the laws of their own countries.

January — June Prev document — Next Document. Sobre el requisito de respuesta adecuada, respuesta adecuada [responsiveness] ver London, A.

Ver especialmente Autor b. The doctor can combine clinical research with professional care, the objective being declaracion de helsinki acquisition of new medical knowledge, only to the extent that clinical research is justified by its therapeutic value for the patient.

Consideraciones sobre las obligaciones posinvestigación en la Declaración de Helsinki

Received 04 January declaracion de helsinki, Accepted declaracion de helsinki January Call for Papers The Editorial Board of Bioethics UPdate invites you to become an active part of this journal encouraging you to submit your manuscripts.

In defense of the vulnerable in medicine and the life The Declaration of Helsinki should be a mandatory, rather than helsinkki, undertaking to comply, included in all the Consent Letters for participation in research trials by any declaracion de helsinki being. Ezekiel Emanuel, fue jefe del Departamento desde hastay fue declaracion de helsinki por Christine Grady quien es la actual jefa del Departamento.