BARC Data Management

All trials are integrated into a single global study database accessible online to the sponsor. BARC’s reporting system facilitates easy adaptation to trial-specific needs such as :

•  duplicate reporting units (classical or SI) 
•  evaluation boxes 
•  alert flagging 
•  blinding 
•  monitoring of inclusion and exclusion criteria linked with laboratory tests. 

Reports are faxed and/or emailed promptly and automatically to the investigator. 

Our offer includes:

• Safety results reported within 24 hours (after reception of the samples)
• Web tools and remote data access  
• Electronic data transfer in most formats