The Single Interface® Preview
Not just developing software for its own sake, but based on needs, leading to innovations: 15 US patents (238 claims) with broad applicability
Learn more15 years of clinical operations experience, from Phase I to Phase IV, in hundreds of trials in every major therapeutic area. Personnel with decades of clinical trial and engineering know how
Learn moreOur systems are validated and delivered according to US and International regulations, such as 21 CRF Part 11/Annex 11 and ICH GCPs
Learn moreWe are so confident in the value we provide that we offer a 100% no-questions-asked money back guarantee
Learn moreThe implementation period of the Single Interface™ is 2-6 weeks, it is our responsibility to launch the entire system ourselves, including data integrations and even mid-study
Learn moreThe Single Interface™ provides early observations of aggregated data for reconciliation, taking advantage of tools and systems integrations to support holistic views and timely role-based reporting
Learn moreAutomate labor-intensive manual tasks to proactively manage key deliverables and enable predictive modeling so you are always one step ahead
Learn moreAggregated data is normalized, reconciled and reported with as much automation as possible, including triggered alerts and other role-based messaging
Learn moreCase Report Forms, Diagnostic Data (Images, Central Reader Reports), Patient Reported Data (i.e. ePRO), Central Safety Lab Data, Central Specialty Lab Data (e.g. Immunology Laboratory Data, Pharmacokinetic Data and Biomarker Data), Central Rater Data, Safety Data.
Randomization Data, Investigational Product Data, Supply Logistics Data, Essential Documents, Monitoring Reports, Monitoring Visits, Queries, Query Status, Timeline milestones, SDV Data.
Site Budgets, Vendor Budgets, Site Invoices, Vendor Invoices, Percentage of Completion
The Single Interface™ gives you single-access to all your data.
Take a look at what past customers have to say or talk to a technology expert now.