Managing External Data Sources in Clinical Trials: Current and Future Strategies

As clinical trials are incorporating an increasing number of sources of non-case-report-form (CRF) data from wearable devices and various laboratories, management of clinical data must address larger, disparate volumes of external data sources. These non-CRF clinical data can cause delays in resolving queries and can place additional burden on eCRF data managers. Efficiently managing this level of complexity and avoiding delays in reaching database lock requires a strategic approach that can track, QC, reconcile and ensure the veracity of a rapid inflow of non-CRF data. Watch this webinar as our thought leaders discuss best practices for dealing with these complex data structures and implementing a data strategy that not only addresses needs for today, but also explores future tactics for proactively optimizing management of external data sources.