Program for Appropriate Technology in Health (PATH)
This sponsor has funded 1 studies across 3 countries.
| EU PAS ID | Status | Title | Protocol uploaded | Results uploaded |
|---|---|---|---|---|
| 45288 | Finalised | 115055-A prospective study to estimate the incidence of diseases specified as adverse events of special interest, of other adverse events leading to... | Yes | No |
PAS by Risk Management Plan (RMP) requirement
Program for Appropriate Technology in Health (PATH)
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
Program for Appropriate Technology in Health (PATH)
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
Program for Appropriate Technology in Health (PATH)
3 Study countries specified are the following:
- Burkina Faso
- Ghana
- Kenya