MDM S.p.A.

This sponsor has funded 1 studies across 4 countries.

PAS funded by this sponsor.
EU PAS ID Status Title Protocol uploaded Results uploaded
11765 Finalised Yes Yes

PAS by Risk Management Plan (RMP) requirement

MDM S.p.A.

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.