Trial Event Services

Cardiabase's Trial Event Services

Through its Central Management of Clinical Dossiers Services, Cardiabase providesinnovative solutions to capture trial events and guide critical event-based protocol decisions. Our solutions support the work of various committees involved in a clinical trial, such as the data and safety monitoring board (DSMB), critical event or endpoint adjudication committee and steering committee. They also improve information sharing among experts, sponsors and the medical community at large.

• Event tracking through the creation of a study-specific event database
   
• In-time dynamic event reporting.
   
• Collection of source documents
   
• Blinding of source documents even for imaging data
   
• Archiving of source documents

Did you know it ?

Good Clinical Practices require that, in addition to treatment assignment, patient-related demographic data be blinded to all parties involved in a clinical trial, including sponsor representatives and experts.

Failure to do so invalidates all data associated with this patient. Therefore we imperatively take great care to blind all information that could identify the patient.