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 applicabilityLearn more
15 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 howLearn more
Our systems are validated and delivered according to US and International regulations, such as 21 CRF Part 11/Annex 11 and ICH GCPsLearn more
We are so confident in the value we provide that we offer a 100% no-questions-asked money back guaranteeLearn more
The 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-studyLearn more
The 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 reportingLearn more
Automate labor-intensive manual tasks to proactively manage key deliverables and enable predictive modeling so you are always one step aheadLearn more
Aggregated data is normalized, reconciled and reported with as much automation as possible, including triggered alerts and other role-based messagingLearn more
Case 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.
On-tap Analytics, Dashboards and Visualizations on everything, including Visual Patient Profile and ad-hoc report building.
Randomize patients dispense study drug and track investigational product distribution, reconciliation & destruction
Receive, process and generate reports for safety events with auto-populated MedWatch or CIOMs forms
Obtain real-time, real-world patient efficacy and safety data to improve quality and compliance
Take a look at what past customers have to say or talk to a technology expert now.