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News Daily News

TCTMD’s Top 10 Most Popular Stories for December 2017

Shelley Wood

December 28, 2017

News Daily News

Meta-analysis: PFO Closure Beats Medical Therapy Alone in Preventing Recurrent Stroke

Yael L. Maxwell

December 22, 2017

News Daily News

FDA Takes on 3-D Printing in Healthcare With Initial Guidance Document

Yael L. Maxwell

December 06, 2017

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for November 2017

Shelley Wood

November 29, 2017

News Conference News AHA 2017

Accelerator-2: Streamlined Regional STEMI Care Speeds Up Treatment, Lowers Mortality

Michael O'Riordan

November 14, 2017

News Conference News TCT 2017

Selection Bias? Debate Asks How Many TAVR Devices Centers Should Stock

Yael L. Maxwell

November 09, 2017

News Daily News

Positionable Shields Slash Radiation Exposure to Cath Lab Staff by Two-Thirds

L.A. McKeown

November 08, 2017

Presentation TCT 2017

Use of NCDR Registries to Evaluate Race and Gender Issues Related to Medications and Devices

Presenter: Alice K. Jacobs, Spencer B. King III, John C. Messenger

October 31, 2017

News Conference News TCT 2017

Intermediate-Risk TAVR Substantially More Cost-effective Than Surgery

Yael L. Maxwell

October 31, 2017

News Conference News TCT 2017

3-D Printing Opportunities Emerge for Cardiologists, Hospitals, and Device Companies Alike

Yael L. Maxwell

October 31, 2017

Presentation TCT 2017

EFS Experiences and Recommendations: A Major Device Company Perspective

Presenter: Andrew Farb, Aaron V. Kaplan, Donald E. Bobo Jr

October 30, 2017

Presentation TCT 2017

The Landscape of CV Device Innovation for Children: Regulatory View

Presenter: Nicole Ibrahim, Satoshi Yasukochi, Sara Takahashi

October 30, 2017

Presentation TCT 2017

FDA Perspectives: Diversity in Clinical Trials and its Impact of Device Evaluation

Presenter: Wayne B. Batchelor, George A. Mensah, Christopher J Popma

October 30, 2017

Presentation TCT 2017

The Landscape of CV Device Innovation for Children: Regulatory View

Presenter: Nicole Ibrahim, Satoshi Yasukochi, Nicole Milligan

October 30, 2017

Presentation TCT 2017

The Landscape of CV Device Innovation for Children: Industry View

Presenter: Nicole Ibrahim, Satoshi Yasukochi, Lisa Becker

October 30, 2017

Presentation TCT 2017

CMS Perspectives on Post-Approval Device Evaluation(Including NEST) and Reimbursement

Presenter: Mitchell W. Krucoff, John C Laschinger, Daniel A Canos

October 30, 2017

Presentation TCT 2017

The Landscape of CV Device Innovation for Children: Industry View

Presenter: Nicole Ibrahim, Satoshi Yasukochi, Declan Dineen

October 30, 2017

Presentation TCT 2017

Current CV Device Use and Unmet Needs in Children: US Academic View

Presenter: Nicole Ibrahim, Satoshi Yasukochi, Frank F. Ing

October 30, 2017

Presentation TCT 2017

Can Post-Approval Registries Inform Device Label Expansion? The TVT Case Example

Presenter: Mitchell W. Krucoff, John C Laschinger, E. Murat Tuzcu

October 30, 2017

Presentation TCT 2017

Current CV Device Use and Unmet Needs in Children: Japanese Academic View

Presenter: Nicole Ibrahim, Satoshi Yasukochi, Hideshi Tomita

October 30, 2017

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TCTMD’s Top 10 Most Popular Stories for December 2017

Meta-analysis: PFO Closure Beats Medical Therapy Alone in Preventing Recurrent Stroke

FDA Takes on 3-D Printing in Healthcare With Initial Guidance Document

TCTMD’s Top 10 Most Popular Stories for November 2017

Accelerator-2: Streamlined Regional STEMI Care Speeds Up Treatment, Lowers Mortality

Selection Bias? Debate Asks How Many TAVR Devices Centers Should Stock

Positionable Shields Slash Radiation Exposure to Cath Lab Staff by Two-Thirds

Use of NCDR Registries to Evaluate Race and Gender Issues Related to Medications and Devices

Intermediate-Risk TAVR Substantially More Cost-effective Than Surgery

3-D Printing Opportunities Emerge for Cardiologists, Hospitals, and Device Companies Alike

EFS Experiences and Recommendations: A Major Device Company Perspective

The Landscape of CV Device Innovation for Children: Regulatory View

FDA Perspectives: Diversity in Clinical Trials and its Impact of Device Evaluation

The Landscape of CV Device Innovation for Children: Regulatory View

The Landscape of CV Device Innovation for Children: Industry View

CMS Perspectives on Post-Approval Device Evaluation(Including NEST) and Reimbursement

The Landscape of CV Device Innovation for Children: Industry View

Current CV Device Use and Unmet Needs in Children: US Academic View

Can Post-Approval Registries Inform Device Label Expansion? The TVT Case Example

Current CV Device Use and Unmet Needs in Children: Japanese Academic View

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