Consentimiento informado en las investigaciones clínicas: una aproximación en pediatría
García Luis, Mileidy; Ropero Toirac, Ramón; Ortiz, Rosa María; Renó, Jesús S.
Bioética (La Habana)
; 5(1): 11-13, 2004.
Artículo en Español | Bioeticacol | ID: bic-3265
Documentos relacionados
Research and research ethics committees and the obligation for them to operate in accordance with the principle of the social covenant.
Do we really know how many clinical trials are conducted ethically? Why research ethics committee review practices need to be strengthened and initial steps we could take to strengthen them.
Community Review Boards offer a path to research equity.
How to streamline the low and negligible research ethics and governance review process from 80 to 10 days: submission to decision.
Professional and academic profile of the Brazilian research ethics committees.
IRBs and the Protection-Inclusion Dilemma: Finding a Balance.
Reasonable disagreement and the justification of pre-emptive ethics governance in social research: a response to Hammersley.
Redundant trials can be prevented, if the EU clinical trial regulation is applied duly.
Included but Still Invisible?: Considering the Protection-Inclusion Dilemma in Qualitative Research Findings.
Don't Ask Too Much: Non-maleficence as the Guiding Principle in IRB Decision-Making.