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PROpartner™ Program for Clinical Research Organizations (CROs)
invivodata works collaboratively with the world’s leading CROs to provide sponsors with added confidence in the execution of their global trials and to ensure our joint processes, timelines and deliverables of the complementary yet interdependent services are managed effectively and efficiently. This reduces both risk and cost for our mutual customers.
invivodata trains, certifies and supports CRO clinical trial service providers through our PROpartner™ program, enabling CROs to successfully monitor trials using our EPX ePRO Management System and to deliver the highest level of service – consistent with the expectations of our customers.
Read recent news on invivodata's partnerships with leading CROs, including:
- “Ahead of the ePRO Curve”; Applied Clinical Trials; Jan. 21, 2010. This article reviews the momentum in the pharmaceutical industry toward the use of PRO data in clinical trials, including the FDA’s publication of a final PRO Guidance and Quintiles’ selection of invivodata as itsprimary preferred provider of ePRO solutions.
- “Quintiles, invivodata Partner”; ClinPage; Jan. 20, 2010. This article covers the impact of the invivodata-Quintiles partnership, and reviews other industry trends on PROs, including the implications of the FDA’s final PRO Guidance and how sponsors are benefiting from capturing ePRO data at earlier phases of clinical development.
For more information about invivodata’s PROpartner™ program for CROs, please contact us today.