CIOMS cited

Heterogeneity of national legislation and practice on clinical trials with vulnerable patients based on the EU Clinical Trials Directive by the example of adults permanently incapable of giving informed consent

Guidance for ensuring fair and ethical broad consent for future use. A scoping review protocol.

Risk of Secondary Distress for Graduate Students Conducting Qualitative Research on Sensitive Subjects: A Scoping Review of Canadian Dissertations and Theses

Risk Management for the 21st Century: Current Status and Future Needs (A collaborative commentary)

Cohort event monitoring of COVID-19 vaccine safety in Europe using patient-reported outcomes: a template protocol from the ACCESS project

Principles of benefit-risk assessment: A focus on some practical applications

Managing ancillary care in resource-constrained settings: Dilemmas faced by frontline HIV prevention researchers in a rural area in South Africa