CHU de Nantes
This sponsor has funded 2 studies across 1 countries.
| EU PAS ID | Status | RMP requirement | Title | Protocol uploaded | Results uploaded |
|---|---|---|---|---|---|
| 18319 | Finalised | Not included in RMP | Pleural disorder caused by Protein Kinase Inhibitor: Disproportionality analyses and identification of cellular target from the World Health... | No | No |
| 37270 | Finalised | Not included in RMP | Deaths and life-threatening events associated with paliperidone palmitate in France | No | No |
PAS by Risk Management Plan (RMP) requirement
CHU de Nantes
The RMP for a medical product outlines strategies to identify, assess, and mitigate risks, including PAS for further evaluation.
Category 1 studies are imposed as condition of marketing authorisation.
Category 2 studies are imposed as specific obligation of marketing authorisation.
Category 3 studies are required under other circumstances.
PAS by study status
CHU de Nantes
The study status is defined according to the timeline dates specified.
Planned studies have not collected any data yet.
Ongoing studies collect data and should publish protocols as soon as possible.
Finalised studies should publish results in the first two weeks after finalisation.
Countries
CHU de Nantes
1 Study countries specified are the following:
- France