The pandemic has made remote trials quite attractive. However, most EDC tools still require specialised teams for setting up the Trial Database, eCRFs with edit checks and annotations etc. In addition, the time taken from LPLV (Last Patient Last Visit) to Database lock is quite high, taking up to 3 months in many cases.
Building and managing trials is cumbersome. Consumes time and effort during the Trial preparation phase.
Data quality is a concern, error prone and does not scale as the number of sites or subjects increase.
Protocol updates during trials introduce additional delays in trial completion.
Data mapping and re-keying, replicating data entry on different systems, inconsistent trial data and late reporting.
Data quality issues cause submission delays and requires additional effort for quality checks and cleansing.
Data extraction and report submission is cumbersome requiring additional data mapping and conversion efforts.
At Datafoundry, we feel that enabling trial setup and data capture in a simple, user-friendly manner is an achievable goal – even for complex trials. We have built DF mTrials AI and DF ePRO AI as the first solution in our Clinical Trials product line.
DF mTrials AI, EDC with Randomization and ePRO is a modern SaaS solution that can get you started on your clinical trial much faster than other tools in the market. The fully configurable product does not need a Clinical DB Programming team to setup the trial. Creating an eCRF is so easy that your trial team need not wait for weeks to enroll subjects and get started. DF mTrials AI brings forward a powerful set of tools to help customers harness data technology to turn research into reality.
30% increase in staff productivity with lesser time spent on getting data ready for analysis.
Up to 50% reduction in SDTM conversion time. Reduce trial start to finish turnaround time reduction and risk mitigation.
UI driven study build, real-time protocol changes and SDTM mapped output.
With MedDRA inbuilt, the records are maintained with standardised medical terminologies.
Available as SaaS hosted on fully compliant cloud. Enables compliance to Part 11, Privacy and Security controls.
Clinical trials for medicinal products, cosmetics, nutraceuticals and medical devices. From simple observational studies to complex Late Phase or Post Marketing studies.