Informed consent in clinical trials with reference to information disclosure to patient-subjects

Introduction The aim of this study was to examine the aspect of information disclosure by doctor investigator during the process of obtaining informed consent in clinical trials.Methods This research employed a mixed-method data collection that is library research and interview.A qualitative methodo...

Täydet tiedot

Bibliografiset tiedot
Päätekijät: Yusof, Yuhanif, Che Ngah, Anisah, Mohamad Zaher, Zaki Morad
Aineistotyyppi: Artikkeli
Kieli:English
Julkaistu: Department of Community Health, Universiti Kebangsaan Malaysia Medical Center 2014
Aiheet:
Linkit:https://repo.uum.edu.my/id/eprint/12895/1/vol%204.pdf