PRO & ePRO Data for Clinical Trial Research

DiaryPRO 170_In Use invivodata’s scientists defined the electronic patient reported outcomes (ePRO) industry over 20 years ago. Since that time, invivodata has evolved into the industry's only fully-integrated Patient Reported Outcomes (PRO) solutions organization. invivodata delivers both strategic consulting services, via the PRO Consulting® division, as well as practical ePRO solutions to biopharmaceutical companies who depend upon patient-centered research in their clinical trials. From crafting PRO measurement strategy, to collecting PRO data electronically with DiaryPRO, our electronic patient diary and SitePRO, our site-based ePRO device, invivodata helps its customers strategically use patient reported data to support labeling claims, enhance market access, and meet other clinical program objectives. Through partnerships with leading CROs and eClinical technology providers, invivodata seamlessly integrates into the clinical ecosystem, helping to minimize operational risk and maximize efficiencies. invivodata’s solutions have been used in over 350 clinical programs, 67 countries, 105 languages and dialects and are built upon the industry-leading ePRO system in delivering primary efficacy data for global drug approvals. Our PRO Consulting services have been used in nearly 300 clinical programs.