invivodata Overview

invivodata offers fully-integrated COA solutions (which includes PROs, ClinROs, and ObsROs) to our customers. These services begin with our PRO Consulting division, which offers COA measurement strategy, instrument selection / development / validation, instrument migration from paper to electronic format, and regulatory approval support. For more information on PRO Consulting, please visit www.patientreported.com.

Once a sponsor is ready to begin collecting patient data electronically, invivodata can collect the data with DiaryPRO – our electronic patient diary, or with SitePRO – our site-based ePRO / eClinRO / eObsRO device. Once the data is collected from the patient, all data is viewable by sites and sponsors via EPX™, invivodata’s web-based clinical oversight system.

For over 25 years, our scientists have combined scientific and regulatory expertise and innovative technology to ensure that the data captured by invivodata is of the highest quality to support labeling claims, enhance market access, and meet other clinical program objectives. Sponsors working with invivodata benefit from this strong scientific and regulatory foundation on which invivodata’s solutions are based, providing confidence that the data we collect will help you reach your goal.

We believe that invivodata provides the best possible service and support in the industry. We are dedicated to continuously improving our solutions to meet the evolving COA and eCOA needs of clinical researchers. Satisfied customers, more than anything else, determine our continued success.