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