RWE-Driven MedTech: Cross-Sector Perspectives on Building Cost-Effective Clinical Evidence Strategies

“RWE‑Driven MedTech: Cross‑Sector Perspectives on Building Cost‑Effective Clinical Evidence Strategies.”

Organized by 3Aware, this virtual event will take place on April 29 and will bring together leaders across the MedTech ecosystem — Notified Bodies, manufacturers and CRO partners — to discuss faster, more efficient and regulatory‑grade clinical evidence strategies.

This year, Marie Abdallah, Compliance Division Director at GMED, will speak during the session:
“From Linked Data to Notified Body Decisions: EU MDR Updates & What ‘Regulatory‑Grade RWE’ Looks Like in Practice.”
She will share the perspective of a Notified Body on how Real‑World Evidence (RWE) can support robust MDR decision‑making.

We look forward to joining this high‑value discussion on innovative, data‑driven approaches to clinical evidence generation.

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