Resource Center

ePRO_Resoureinvivodata is committed to  sharing with the industry the knowledge we have gained in over 20 years of capturing valid and reliable PRO data electronically.  Through this ePRO Resource Center, we hope to answer many of the questions that clinical trial sponsors have about effectively using ePRO in clinical development and  to provide the latest regulatory, scientific, and industry information on PROs in clinical research.

Select a link from the below list for more information.

Additionally, take advantage of invivodata’s PROficiency™ educational series, which enables researchers to continually advance their knowledge of patient reported outcomes and stay up-to-date on the PRO regulatory environment.