Strengthening your care for patients
Industry experts share the latest interventional techniques and provide their advice on how best to adopt them within clinical practice.About our programs
Edwards Benchmark Program
Our program may support your heart centre in optimising its transcatheter aortic valve implantation (TAVI) care pathway for better patient outcomes.Learn more
Tips and Techniques
Explore case recordings, expert-delivered educational videos on procedural challenges, tips and techniques, peer interviews and more.View videos
Edwards Learning Network, an educational portal for healthcare professionals providing continuous learning and development in structural heart intervention.Find out more
The latest transcathether heart valve in the
The first TAVI valve to receive a CE mark for severe aortic stenosis (sAS) patients at low surgical risk.
Edwards valve proving non-inferior to surgery on mortality and stroke in the PARTNER IIA Trial.1
Learn how the Edwards clinical trial programme has shaped the aortic stenosis treatment landscape.
Uncover the wide-ranging economic and quality of life benefits possible with the Edwards SAPIEN 3 transcatheter heart valve.4
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1. Leon MB, et al. N Engl J Med 2016;374:1609-1620 and supplementary material.
2. Leon MB, Smith CR, Mack M, et al; PARTNER Trial Investigators. Transcatheter aortic-valve implantation for aortic stenosis in patients who cannot undergo surgery. N Engl J Med 2010;363:1597-607.
3. Smith CR, Leon MB, Mack MJ, et al.; PARTNER Trial Investigators. Transcatheter versus surgical aortic-valve replacement in high-risk patients. N Engl J Med 2011;364:2187-98.
4. Cohen DJ. Economic Outcomes of TAVR vs SAVR for Low-Risk Patients: Results from PARTNER 3 Trial. Presented at TCT 2021, Orlando Fl. November 5th 2021.
For professional use. For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use (consult eifu.edwards.com where applicable). Edwards devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.