Solutions for Capturing Patient Data

For over 25 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.

Now that the FDA has extended the 2009 PRO Guidance to all Clinical Outcome Assessments (COAs), you can trust invivodata – the leading experts on the PRO Guidance – to help you with your overall COA strategy, including PROs, ClinROs, and ObsROs.  

We’re committed to making every trial a success – so we’ve designed our eSolutions 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 / eClinRO / eObsRO 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 eSolutions to capture primary endpoints in regulatory approvals that have been approved by the FDA, EMA, and PMDA.

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 Services
Our clear collaborative research effort that makes the collection of patient, clinician, and ovserver reported outcome 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 to improve clinical outcome assessment data collection and clinical trial management.