Are your legacy studies trapped in static formats?
Studies conducted before the SDTM mandate are often only available in digital forms like PDF. If those legacy studies hold value today—for repurposing, safety signaling, or exploratory analysis—there is no easy way to digitally access or analyze them.
Most Sponsors' legacy trial data do not easily render an integrated patient profile if a scientific query, audit, or regulatory agency question arises.
THE CHALLENGE
"Prior to working with a top ten pharmaceutical, it took their programmers well over a year to digitize 4 legacy trials. The current digital source data requires costly curation, reprocessing and time before transformation into an analysis ready digital data repository."
The "Nightmare" of Legacy Retrieval
-
📦Retrieving study documents (Protocol, CSR, CRF, SAP)
-
📦Manual transcription errors and validation needs
-
📦Inconsistent terminology across decades
-
📦Lack of metadata for meaningful search
-
📦Inability to perform cross-study analysis
Rapid 3-5 Week Turnaround
We offer sponsors a 3-5 week turnaround. Our approach in digitizing legacy clinical studies enables a fully query-able, analysis-ready dataset that can be warehoused either on a secured instance of PointCross XBIOM™ analysis workbench or in a target model outlet suitable for your internal repository.
Flexible Warehousing
Hosted on XBIOM™ or delivered to your own data lake.
SDTM Target Models
Automated transformation to SDTM target models for regulatory compliance.
Cost-Effective Strategy
Supported several Sponsors in re-thinking their warehousing strategy.
Ready to modernize your legacy data?
We offer a firm fixed price once you share the required resources under an NDA. Stop letting valuable data gather dust.
