Programa públic d'analítica de dades per a la recerca i la innovació en salut (PADRIS)
This sponsor has funded 1 studies across 1 countries.
| EU PAS ID | Status | Title | Protocol uploaded | Results uploaded |
|---|---|---|---|---|
| 48017 | Planned | Risks of pharmacological interactions of direct oral anticoagulants: thrombotic and hemorrhagic events leading to hospital admission in Catalonia.... | No | No |
PAS by Risk Management Plan (RMP) requirement
Programa públic d'analítica de dades per a la recerca i la innovació en salut (PADRIS)
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
Programa públic d'analítica de dades per a la recerca i la innovació en salut (PADRIS)
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
Programa públic d'analítica de dades per a la recerca i la innovació en salut (PADRIS)
1 Study countries specified are the following:
- Spain