Food and Drug Administration (FDA)
This sponsor has funded 2 studies across 2 countries.
| EU PAS ID | Status | Title | Protocol uploaded | Results uploaded |
|---|---|---|---|---|
| 36240 | Ongoing | Registry to study factors that may impact COVID-19 occurrence and severity (CARE) | No | No |
| 48616 | Ongoing | Bayesian Evaluation of Time-To-Event and Reliability (for vaccine surveillance) (BETTER) | Yes | No |
PAS by Risk Management Plan (RMP) requirement
Food and Drug Administration (FDA)
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
Food and Drug Administration (FDA)
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
Food and Drug Administration (FDA)
2 Study countries specified are the following:
- United Kingdom
- United States