Our vision is to be the leading organization within the health technology and medical device ecosystem for conducting efficient and timely high-quality real-world evidence (RWE) studies throughout the total product life cycle (TPLC).
Our mission is to catalyze the timely, reliable, and cost-effective development of Real-World Evidence to enhance regulatory and clinical decision-making.
The U.S. Food and Drug Administration (FDA) today announced that the National Evaluation System for health Technology Coordinating Center (NESTcc), an initiative of the Medical Device Innovation Consortium (MDIC), has achieved recognition as one of the first collaborative communities with participation by the FDA’s Center for Devices and Radiological Health (CDRH). CDRH identified participation in […]
https://nestcc.org/wp-content/uploads/2019/08/new-logo-300x219.png00Natalie Rosehttps://nestcc.org/wp-content/uploads/2019/08/new-logo-300x219.pngNatalie Rose2019-09-20 18:41:132019-09-26 19:40:22NESTcc Named One of the First Collaborative Communities with FDA Participation
The National Evaluation System for health Technology Coordinating Center (NESTcc) is soliciting applications for new Network Collaborators to apply to join the NESTcc Data Network. This opportunity is open to organizations that have access to high-quality real-world data (RWD) and expertise in research with RWD in order to support improved evidence for medical devices throughout the medical […]
Today, NESTcc announced 12 new Real-World Evidence (RWE) Test-Cases. These projects will answer questions of importance to the medical device ecosystem through collaborations between NESTcc Network Collaborators and submitting organizations, including health systems, government organizations, non-profit patient organizations, and medical device manufacturers. NESTcc’s Test-Case portfolio now includes 20 projects that span the Total Project Life Cycle […]