If you decide to choose the full-service setup of your trial, the following points will be attended to by our Professional Services Team:

• Creation of the eCRFs incl. queries
• Creation of users, roles and access rights
• Creation of online reports and data export routines
• Customization of enhanced requirements like randomization, drug accountability and logistics, metadata and libraries
• Modification of the separate patient identification database
• Configuration of the laboratory data import