Responses
Other content recommended for you
- Analysis of the status of informed consent in medical research involving human subjects in public hospitals in Shanghai
- How to handle informed consent in longitudinal studies when participants have a limited understanding of the study
- Subjects’ views of obligations to ensure post-trial access to drugs, care and information: qualitative results from the Experiences of Participants in Clinical Trials (EPIC) study
- What is the role of the research ethics committee? Paternalism, inducements, and harm in research ethics
- Fair subject selection in clinical research: formal equality of opportunity
- Diversity in clinical research: public health and social justice imperatives
- Scientific research is a moral duty
- A critical appraisal of clinical trials conducted and subsequent drug approvals in India and South Africa
- Screening and Evaluation of Study Subjects in Patient-Oriented Research
- Assent for children's participation in research is incoherent and wrong