Recurring concern
Inadequate informed-consent processes for medical treatment
- Reports that mention this concern
- 31
- Times this concern has been raised
- 37
- Stated actions linked to this concern
- 56
What this concern includes
Includes failures of medical-treatment consent processes, including initiation, information about material risks, time for consideration, consistency of procedure, assessment of consent and documentation, where the failure is directly tied to obtaining valid informed consent.
What is not included
- Excludes legal-status or detention transfers that do not concern consent to medical treatment.
- Excludes general communication, training, documentation or staffing deficiencies unless they are directly tied to the medical-treatment consent process.
- Excludes clinical assessment or treatment-selection failures that do not concern obtaining or recording informed consent.
Trends
Reports over time
Reports mentioning this concern, over time
Reports about this concern issued each year.
* 2026 is projected from reports observed to 7 Sep 2026.
Most frequent recipients
Most frequent recipients
Reports about this concern sent to each recipient.
Reports and published responses 31 reports
See individual reports that have raised this concern, and the actions taken in response
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Concerns raised1
Insufficient time for trial information review and informed consent before procedures
This report raised 7 other concerns. They are not shown here because they do not form part of this recurring concern.
No linked response statementsNo respondent-stated action or position is linked to these concerns in the published data.
Actions and positions describe what organisations say in published responses. Implementation is not independently verified.
Data last updated 7 September 2026