Informed Consent in Clinical Trials with Reference to Information Disclosure to Patient-Subjects.

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. This research employed a mixed-method data collection that is library research and interview. A qualitative methodology and analysi...

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Bibliographic Details
Main Authors: Yuhanif Yusof, Anisah Che Ngah, Zaki Morad Mohamad Zaher
Format: Article
Language:English
Published: Universiti Kebangsaan Malaysia 2014
Online Access:http://journalarticle.ukm.my/7125/1/vol_4_no_1_2014_49.pdf