Coordinator: Rosa M. Antonijoan email@example.com
Staff: Ma Rosa Ballester Judit Claramunt Susana Clos Sonia Coma Ma Ángeles Funes Consuelo García Ignasi Gich Sandra Giménez Ana Gomis Mireia González David Martínez Joan Martínez Maribel Martínez Pura Martínez Esteve Mercader Sara Mora Montserrat Puntes
Perform clinical drug trials and/or clinical research in compliance with methodological, ethical and legal requirements in the context of international Good Clinical Practice guidelines concerning:
Clinical trials that are not of therapeutic interest for participants (phase I, special populations, psychopathological research, biomarkers, proof of concept).
Clinical trials in neuropsychopharmacology.
Clinical trials in initial developmental phases.
Three separate work areas have been designated for the trials:
24 beds distributed in 4 units: trials in healthy volunteers and patients.
2 individual rooms for CNS studies.
4 consulting rooms for complementary testing mainly related to CNS.
3 cubicles to evaluate psychomotor performance.
Logistic support area:
Rest area for clinical trial participants with bathrooms and kitchen.
Areas for the preparation, centrifugation, and separation of biological samples.
Management, administration and data processing:
Area for monitors.
IT equipment for clinical trial activities of a non-experimental nature.
Coordinator: Rosa M. Antonijoan E-mail: RAntonijoana@santpau.cat