Data Management

Distribution and Collection of Data Discrepancies

BMA will distribute and collect data discrepancy queries within an average of 7-14 days from clinical sites in the Americas and throughout the world. During the life of a clinical trial and, most importantly, at interim and final deadlines, the timely return of accurate data is crucial. BMA can help ensure that, through constant communication with clinical sites and monitors, your clinical trial is not jeopardized.

Serious Adverse Event Narratives and Reconciliation

Serious Adverse Event retrieval for timely reporting to Regulatory Authorities, as well as writing SAE Narratives and Reconciliation, are prepared according to sponsor specifications.

CRO Interaction and Monitoring

Through our extensive experience with major CROs, metrics for data management of study data can be developed, as well as monitored to ensure on-time delivery of clinical data to meet sponsor deadlines.