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CTSI Watch and Learn: FDA 101: A Primer on IDEs
Three 510(k) tips
What Is An Investigational Device Exemption (IDE)?
Understanding the Investigational Device Exemption (IDE) Process
How is CDRH encouraging more US-based first-in-human studies?
MDICx: EFS Site Best Practices: Implementation Strategies from the Sponsor Perspective
Building a New Medical Device (or Evolving an Existing One) with Regulations in Mind
SYS-009 Clinical Procedure
2023 TOP FDA Diagnostic Data Solutions Showcase
Indiana CTSI Winter Retreat: Translational Pathway Sessions
Indiana CTSI Winter Retreat: Digital Health and Wearable Devices Workshop
Accelerating Time to Market with Early Feasibility Studies
