Proving Performance: Real-World Comparator Studies for #MedTech. In our latest article, we demonstrate how to produce head-to-head regulatory-grade RWE, using #EHR-derived data for #MedicalDevices. 👉 hubs.ly/Q03DncvN0
📢 Label Expansion Support Features #3Aware helps #MedicalDevices manufacturers unlock new indications & expediate new market access with regulatory-grade RWE. See it in action! hubs.ly/Q03BpRRC0 & Book a DEMO: hubs.ly/Q03BpSs80
🎥 Check out this exclusive clip about NEST Data Mark! Key takeaways: ✅Structured review of RWD relevance and reliability for this pilot ✅Medical Device RWE Marketplace initiative🔗Access the full webinar: hubs.ly/Q03zCW080#RealWorldEvidence#MedicalDevices
Congratulations to our Co-Founder, @bradbostic on being named to the @IBJnews 2025 Indiana 250! We’re proud to see his leadership recognized on a statewide level.🔗 See Full List: indiana250.com📰 Read Official Announcement: hubs.ly/Q03yYMz60
🚀 New Board Member 🚀 Cindy Senerchia, RN, MSc, has joined our Scientific Advisory Board! Cindy is a Clinical Trial Solutions Consultant at @Optum , with a background spanning #healthcare operations, RWD architecture, and algorithm validation. Welcome, Cindy!
Webinar Guest Profile 🎙️ Jill Dreyfus, PhD, MPH, joins our webinar, "From RWD to RWE – Industry & Regulatory Insights" Now at NEST/@MDIConline she has over 25+ years of epidemiological research experience. 🔗 Register Here: hubs.ly/Q03qTVXf0#NESTcc#MedicalDevices#3Aware
🎙️ Webinar with Special Guest: NEST/@MDIConline
Dr. Jill Dreyfus joins our upcoming webinar: "From RWD to RWE – Industry & Regulatory Insights" with practical insights, proven frameworks, real-world examples and best practices! Learn More & Register Here: hubs.ly/Q03qTVXf0
⏰ One week to go! Last call for symposium registrations, a few seats are still available. Don't miss this afternoon of regulatory perspectives, manufacturer insights, and #realworlddata innovation! Join us... register now! hubs.ly/Q03cbLN30
The FDA now expects highly reliable & relevant #RealWorldEvidence. Do you still rely on biased (so-called "high quality") surveys and limited chart reviews while clinical EHR data remains untouched, full of untapped insights? Is your RWE strategy aligned with FDA guidance?
Speaker Profile 🎙️ Dr. Ziskoven of @tuvcom_presse brings NB perspective to the RWE-Driven #MedTech Symposium. He'll cover post-market clinical evaluation & structured dialogues, with actual examples. Inform your EU strategy & bring regulatory questions! 🔗hubs.ly/Q03cbLN30
🎙️ Symposium Speaker Profile 🎙️ What went wrong with #EUMDR? @dr_akra will share news from recent EU stakeholder meetings & what lies ahead for acceptance of #RealWorldEvidence. Don't miss it! 📅 April 29th | 1PM - 6 PM 🔗 hubs.ly/Q03cbLN30 🔗
🎙️ Speaker Profile 🎙️ Melanie Lannon (Hansen) of @CONMEDCorp will address challenges of long-term follow-up, #PMCF for #legacydevices, standard of care for outcome measures & the role of RWD/RWE in her work. Bring your notepad & questions! Register Now 🔗 hubs.ly/Q03cbLN30
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