From: Identifying structures, processes, resources and needs of research ethics committees in Egypt
Topics | Percentage of RECs reporting |
---|---|
The use of placebo controlled trials | 100% (10/10) |
Determination of methods to reduce risk | 92% (11/12) |
The interpretation of pre-clinical studies | 91% (10/11) |
Determination of risks in research | 91% (10/11) |
Assessment of benefits to participants and society | 90% (9/10) |
Scientific design issues in clinical trials | 90% (9/10) |
Monitoring and oversight of approved studies | 90% (9/10) |
Assessment of cultural sensitivity for informed consent | 82% (9/11) |
Assessment of understanding of informed consent | 80% (8/10) |
Access to benefits after the trial is over | 78% (7/9) |
Determination of appropriate subject selection in vulnerable populations | 75% (9/12) |
Community participation | 67% (6/9) |
Social and behavioral studies | 75% (9/12) |
Privacy and confidentiality | 70% (7/10) |