Regulatory Requirements for BRS Technology in the US - Andrew Farb, MD

↳ This is a section part of Moment: CRT 2016 Technology & Innovation - BRS Show Me the Data: Insights Into the ABSORB Trials

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Summary

Regulatory Requirements for BRS Technology in the US presented by Andrew Farb, MD at CRT 2016

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Target Audience

  • Interventional Cardiologists
  • Interventional Fellows

Session Name: BRS Show Me the Data: Insights Into the ABSORB Trials

Track: Technology & Innovation

Learning Objectives

  • Update in advances with bioresorbable technologies in interventional procedures

Other Components in this Moment

Overview
ABSORB III: Pivotal Trial Main Results - Gregg Stone, MD, FSCAI
ABSORB III: Trial Sub-group Analysis – Diabetes, Small Vessels, and More - Dean Kereiakes, MD, FACC, FSCAI
ABSORB Japan and ABSORB China - Shigeru Saito, MD, FACC, FSCAI
Latest European Randomized Trial Data: TROFI-2, EVERBRIO, and More - Corrado Tamburino, PhD, FSCAI
What Did We Learn from the Meta-analysis of ABSORB Studies? - Robert Byrne, MB BCh, PhD
DESolve Series of Studies - Stefan Verheye, MD, PhD
The REVA TyrosineDerived Polycarbonate Bioabsorbable Scaffold: Program Update and Lessons Learned - Ricardo Costa, PhD
Update on the BIOSOLVE II Clinical Trial Using DREAMS Absorbable Magnesium Scaffold - Michael Haude, MD, PhD
Real World Usage of BVS in Europe - Corrado Tamburino, PhD, FSCAI
How to Use the BVS Safely: Step-by-step Guidance - Corrado Tamburino, PhD, FSCAI
Regulatory Requirements for BRS Technology in the US - Andrew Farb, MD
PRO: I Am Already Doing it - Alan Yeung, MD, FSCAI
CON: Not So Fast - Ted Bass, MD, MSCAI
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