Respiratory Effectiveness Group (REG)

This sponsor has funded 19 studies across 10 countries.

PAS funded by this sponsor.
EU PAS ID Status RMP requirement Title Protocol uploaded Results uploaded
4238 Finalised Not included in RMP Yes No
4860 Finalised Not included in RMP Yes No
4869 Finalised Not included in RMP Yes No
4891 Finalised Not included in RMP Yes No
4921 Finalised Not included in RMP Yes No
5032 Ongoing Not included in RMP Yes No
8740 Finalised Unspecified No No
10483 Finalised Unspecified Yes No
10679 Finalised Not included in RMP Yes No
10684 Ongoing Not included in RMP Yes No
11656 Finalised Not included in RMP Yes No
12086 Finalised Not included in RMP Yes No
12132 Finalised Not included in RMP Yes No
13959 Finalised Not included in RMP No No
17985 Finalised Not included in RMP Yes No
19984 Finalised Not included in RMP Yes No
21791 Finalised Not included in RMP Yes No
28667 Finalised Not included in RMP Yes No
30625 Ongoing Not included in RMP Yes No

PAS by Risk Management Plan (RMP) requirement

Respiratory Effectiveness Group (REG)

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.