Quality of informed consent in clinical trials

Introduction and objectives Obtaining consent prior to any medical intervention is currently a necessity, the omission of which may lead to litigation. Years of analyses have resulted in strict policies as to what should the patient be informed about and who should provide such information. It would...

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Bibliographic Details
Main Author: Anna Zagaja
Format: Article
Language:English
Published: Institute of Rural Health 2020-03-01
Series:Journal of Pre-Clinical and Clinical Research
Subjects:
Online Access:http://www.journalssystem.com/jpccr/Quality-of-informed-consent-in-clinical-trials,119621,0,2.html