Involving opinion leaders and highly qualified personnel, we organize Advisory Boards that define guidelines and new orientations in different fields: quality control, microbiology, Investigational Medicinal Products (IMPs), pharmaceutical research, clinical research, biotechnologies.
Managing clinical trials, we carry out, further to selection and start up of involved centers, the organization and participation to Investigator’s Meeting:
• we organize and reimburse travels
• we organize banquets
• we elaborate the Operative Manual of the study and distribute it to researchers
• we present the Research Protocol and Case Report Forms (CRF)
• we design simulations of CRF filling and analyze possible difficulties that may arise during the study