Working with stakeholders across the medical device ecosystem to catalyze the timely, reliable, and cost-effective development of Real-World Evidence to enhance regulatory and clinical decision-making.
NESTcc panel at MDIC Annual Public Forum 2017. Watch the session here.
Today, NESTcc announced its first Real-World Evidence Test-Cases. Initially submitted through a public call for concepts in January […]
What is VISION? Stakeholders from every sector stand to benefit from a more complete and efficient method of […]
“I’ve spent my whole career focused on bringing better products to patients who can benefit from them. Patients […]
Join @MDIConline Case for Quality Forum online today to hear @NESTccMedTech Deputy Director @RachelRRath discuss NESTcc Governance: mdic.org/cfq/register/ twitter.com/MDIConline/sta…
We’re looking forward to participating in the @MDIConline Case for Quality Forum on Nov 28. Register to attend in-person or online to hear @NESTccMedTech Deputy Director @RachelRRath discuss NESTcc Governance: mdic.org/cfq/register/ twitter.com/MDIConline/sta…
Read FDA Commissioner @SGottliebFDA and CDRH Director Dr. Jeff Shuren’s statement on enhancing post-market safety and the role of @NESTccMedTech in the #medicaldevice ecosystem: bit.ly/2A7XdNb twitter.com/FDAMedia/statu…
Reflecting on my first year as the Executive Director of NESTcc, it is striking to see the changes and progress that have shaped the Coordinating Center’s priorities in such a […]
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