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We provide clinical trial management services for the pharmaceutical, biotechnology and medical device industries.

The management of a clinical trial is more complicated than it might seem, as many actors are involved (manufacturers, sponsors, ethics committees, competent authorities, centres, foundations, researchers, legal departments, patients…). In addition, we will work under the standards of Good Clinical Practice and Harmonisation Guidelines (GCP-ICH Guidelines) to ensure the quality of the study. Being able to count on us as a partner in which to entrust the management of the study is the best choice. We act as a bridge between the sponsor, your company, and the other actors involved in the conduct of the clinical study.

Throughout the study, work is carried out in accordance with Good Clinical Practice (GCP) to ensure the quality of the study.