SSStudyParticipantsRecruitmentTrialOutcome object

Mandatory to inform participant of clinical trial outcome

No

Additional Information

In informed consent (IC) the participant can be asked if the/she wants to be informed about the study results. If yes, the PI informs him about the results.

This project (ECRIN Integrating Activity/ECRIN-IA) has received funding from the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement no 284395
Feedback