New drug applications are on the rise, presenting new demands at the clinical studies level. Study managers are taking on more responsibilities and the need for properly migrating multi-sourced, multi-type studies into their eTMF regardless of type or complexity is of critical importance. DRS offers best in class solutions to help sponsors and CRO's make sure clinical data is being scanned and entered into eTMF platforms on a timely and efficient basis, allowing for Quality Assurance checks of datasets on a real time basis and certifying results... Clinical studies are complex undertakings that involve the processing and organization of massive amounts of data. When mistakes occur, timely identification and response means that problems can be resolved prior to inspections. DRS offers full end-to-end eTMF auditing designed to discover problems with clinical data collection, attribution and filings of the study documents. Regardless of the eTMF system you are using, DRS provides an..