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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

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