Recursis

We organize data to make analysis easy. Recursis provides professional data visualization, analysis, and automation solutions to help clinical and pre-clinical project teams integrate data. We empower your study teams to analyze, visualize, report, model, and monitor ADME, toxicology, adverse events, labs, dosing, pharmacokinetics, pharmacodynamics, biomarkers, efficacy, patient reported outcomes, and EDC data, all in one place. We can specialize to help you execute oncology data analytics, RECIST, PFS, OS, other study endpoints, and automate at everything scale. 1) We make medical monitoring and project data reviews efficient and effective. -Patient profiles for complete view of key study information, from screening to follow-up. -Monitor safety signals based on labs, adverse events, ECGs, vital signs, physical exams, and ePRO data. -Analyze dosing and exposure data as it relates to study endpoints and efficacy. -Quantify and share key study outcomes in near real-time, as they emerge. -Access fresh data and visuals for effective communications with sites and sponsors. 2) We integrate analytics with any EDC or safety systems: -VEEVA Vault™ CDMS -Medidata RAVE™ EDC -Viedoc Clinic™ -Clincase™ -Oracle Clinical™ -Argus™ -Medrio™ -...and whatever else you have. 3) Analyze and visualize all your clinical study data with precision. -Analyze inclusion and exclusion reasons. -Track screening and enrollment progress. -Understand safety events leading to discontinuations and interruptions. -Visualize efficacy data as it becomes available. -Use PK and PD for exploratory and confirmatory analyses. -Segment responder populations by biomarker data. -Get CTCAE and DAIDS graded safety labs you need for medical monitoring. -Have patient reported outcomes (ePRO) data integrated for analysis. -Integrate medical histories and real world data into your clinical visualizations.