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Bristol-Myers Squibb and Pfizer Enroll First Patient in Phase 4 AUGUSTUS Trial to Evaluate Safety of Eliquis (apixaban) in Nonvalvular Atrial Fibrillation Patients with a Recent ACS or Undrgoing PCI

September 09, 2015

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Symic Biomedical Advances First Product Candidate, SB-030, into Clinical Development with Treatment of First Patient in SHIELD Trial

October 27, 2015

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Early Human Cases With Edwards FORMA Tricuspid Repair System Presented At TCT

October 14, 2015

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Drug Shortage Update: Eptifibatide Injection

September 23, 2015

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MValve Technologies Implants First Human Catheter Based Mitral Valve Replacement System

October 05, 2015

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Biotronik launches 2 new studies

August 13, 2015

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Vascular Solutions Expands Launch of PolarCath(TM) System With 0.035” Catheters

August 03, 2015

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Drug-Coated Balloon Shown To Be Superior To Conventional Angioplasty In Treating Superficial Femoral Artery Disease After Two Years

October 14, 2015

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Mitralign to Provide Update on Transcatheter Tricuspid Repair at TCT 2015

October 12, 2015

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SentreHEART Receives CE Mark Approval for the LARIAT Surgical Left Atrial Appendage Suture Delivery Device

October 08, 2015

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Bristol-Myers Squibb and Pfizer Enroll First Patient in Phase 4 AUGUSTUS Trial to Evaluate Safety of Eliquis (apixaban) in Nonvalvular Atrial Fibrillation Patients with a Recent ACS or Undrgoing PCI

Symic Biomedical Advances First Product Candidate, SB-030, into Clinical Development with Treatment of First Patient in SHIELD Trial

Early Human Cases With Edwards FORMA Tricuspid Repair System Presented At TCT

Drug Shortage Update: Eptifibatide Injection

MValve Technologies Implants First Human Catheter Based Mitral Valve Replacement System

Biotronik launches 2 new studies

Vascular Solutions Expands Launch of PolarCath(TM) System With 0.035” Catheters

Drug-Coated Balloon Shown To Be Superior To Conventional Angioplasty In Treating Superficial Femoral Artery Disease After Two Years

Mitralign to Provide Update on Transcatheter Tricuspid Repair at TCT 2015

SentreHEART Receives CE Mark Approval for the LARIAT Surgical Left Atrial Appendage Suture Delivery Device

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