- | Increasing Study
Sensitivity Early in Trials
- | Choosing between
PDA & IVR FOR ePRO - | Register for
PRO GAP ANALYSIS
- | Download the
FDA's FINAL GUIDANCE ON PROs
invivodata’s scientists defined the electronic patient reported outcomes (ePRO) industry over 20 years ago. Since that time, we have focused on developing innovative ePRO solutions for clinical research that have been used in over 275 clinical trials to collect accurate patient reported outcomes (PRO) data. Our innovations included the revolutionary DiaryPRO, the electronic patient diary and SitePRO, our site-based PRO tool. With the market’s first wireless eDiary solution, automatic patient data uploads, and our development of the space-saving invivodata® EasyCharge™ connector, invivodata has evolved into the ePRO industry’s innovation-leader.
Only invivodata combines the scientific and regulatory expertise needed for ePRO with practical technology and proactive services to maximize your clinical research investment. Trial after trial, our proven ePRO systems enable sponsors to confidently determine the effectiveness of new medical products and therapies.
ePRO Technology Simplified
How do you ensure that ePRO technology is easy-to-use and decreases study team burden?
PRO Consulting
Need expertise in the area of measuring signs and symptoms?
invivodata PROActive Services
What services does invivodata provide to ensure that your ePRO trial runs smoothly?
The PROs of ePRO
Want an industry thought leader’s perspective on PROs and ePRO? Read "The PROs of ePRO" now.