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The process of obtaining informed consent for clinical trials is tightly regulated; complications arise in circumstances when consent may be waived, or when needed from vulnerable populations http://ow.ly/rEMe30j5MVq.

How to obtain informed consent for research

Licari, Amelia
Writing – Review & Editing
2018-01-01

Abstract

The process of obtaining informed consent for clinical trials is tightly regulated; complications arise in circumstances when consent may be waived, or when needed from vulnerable populations http://ow.ly/rEMe30j5MVq.
2018
Medical Research, General Topics covers a wide array of topics in medical and biomedical research, with a specific emphasis on human disease, human tissues, and all levels of research into the pathogenesis of clinically significant conditions. Specific medical fields that are characterized by the inclusion of material from several other specializations are also covered here; these include general and internal medicine, tropical medicine, pediatrics, gerontology, epidemiology, and public health. Resources dealing with specific clinical interventions are excluded and are placed in the Medical Research: Diagnosis & Treatment category. Resources that emphasize the specific disease types, or specific systems affected are also excluded and are categorized according to the pathogen or system pathophysiology.
BREATHE
sì
WOS:000434262800010
2-s2.0-85049607233
Comitato scientifico
Inglese
Internazionale
ELETTRONICO
14
2
145
152
8
29875834
Pulmonary and Respiratory Medicine
http://breathe.ersjournals.com/content/14/2/145.full.pdf
no
2
info:eu-repo/semantics/article
262
Manti, Sara; Licari, Amelia
1 Contributo su Rivista::1.1 Articolo in rivista
none
1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1223617
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