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GMED at the 2026 US Medical Device & Diagnostic Clinical Evidence Conference
24–26 March 2026 | Boston, MA
GMED is pleased to announce that Chris Brodrick, Product Reviewer and SME-Orthopedics, will be speaking at the 2026 US Medical Device & Diagnostic Clinical Evidence Conference, organized by TT LifeSciences, presenting:
“The Quest for ‘Sufficient Data’: Decoding Data Sufficiency and Key Strategies for Collecting Enough Evidence Under the MDR”
Under the Medical Device Regulation (MDR), one of the most critical -and most misunderstood- expectations is demonstrating sufficient clinical evidence.
In this expert session, Chris will explore:
- What “sufficient data” truly means from a notified body perspective
- Common evidence gaps identified during conformity assessments
- Strategies to proactively build robust clinical evidence programs
- Practical approaches to leveraging clinical investigations, PMCF, literature, and real-world data
- How early planning reduces delays and costly remediation
This session is designed for regulatory, clinical, and quality professionals navigating MDR clinical evaluation requirements and seeking greater predictability in their CE-marking strategy.
Click here to register for the event or contact your GMED certification partner to learn more about how we can support your clinical evidence strategy.