Why invivodata
"Every electronic diary vendor can meet the hardware requirements for ePRO, but invivodata does so much more. My first-hand experiences with the invivodata team have shown me how their proactive services really make a difference in keeping studies on track and running smoothly."
Lynne Rowe
Director Clinical Operations, AcelRx Pharmaceuticals , Inc.
Why invivodata
ePRO Knowledge and Insight
For over 20 years, invivodata’s scientists have been studying and improving the process for collecting valid Patient Reported Outcomes (PRO) data to support clinical trials. This experience, coupled with our acknowledged scientific and regulatory expertise, has led to the development of the industry’s most reliable and innovative ePRO solutions.
We’re committed to making each ePRO trial a success – so we’ve designed our ePRO systems with all end-users in mind. We realize that patients and clinical research coordinators have a lot to deal with during a clinical trial – so we’ve introduced user-friendly features that ensure our ePRO systems help them succeed.
Why should you work with invivodata?
Industry Leadership
Discover the difference innovation can make in your clinical trial.
Scientific Expertise
Our assessment approach is consistent and reliable, and is designed to provide a more accurate depiction of a patient’s true status.
Regulatory Understanding
invivodata has implemented our ePRO system to capture primary endpoints in new drug applications (NDAs) that have been approved by the FDA.
Proven Clinical Experience
Our solutions have demonstrated a significant increase in statistical power, as well as decreases in the magnitude of the placebo response.
Unparalleled Operational Insight
Our solutions allow you to monitor and ensure that patients are fully protocol-compliant.
Comprehensive Product Offering
Explore our wide-array of product solutions for capturing field and clinic-based patient data.
ProActive ePRO Services
Our clear collaborative research effort that makes the collection of PRO data as simple as possible for trial sponsors, investigative sites and subjects.
Reliable Data
invivodata delivers over 95% protocol compliance - regardless of patients' technological experience or age.
Contact invivodata today for more information about why you should choose to work with invivodata.