Studies management

 

• We adapt protocols to current regulations and we do selection of investigators (in different therapeutic areas).

 

• We applicate for permissions (Ethics Committees / Health Authorities, Competent Authority) and we manage contracts.

 

• We do initiation and close-out visits and monitoring in situ and follow-up in house.

 

• Support of trial supplies: guides and posters

 

• We offer a call center for receiving adverse events