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The truth about the truth: What matters when privacy and anonymity can no longer be promised to those who participate in clinical trial research?

Patients' Awareness About Their Rights: A Study from Coastal South India

Moral Standards for Research in Developing Countries From "Reasonable Availability" to "Fair Benefits"

Clinical Research in Low-Literacy Populations: Using Teach-Back to Assess Comprehension of Informed Consent and Privacy Information

‚Mirroring‘ the Ethics of Biobanking: What Analysis of Consent Documents Can Tell Us?