September 1, 2009 – CardioDx said last week it successfully completed its multicenter validation study for Corus CAD, the first gene expression test to quantify the likelihood of obstructive(1) coronary artery disease (CAD) in patients with stable chest pain.

August 31, 2009 – IDEV Technologies Inc. announced last week the first patient was enrolled in the company's FDA-approved multicenter clinical trial of its self-expanding SUPERA stent for the treatment of biliary and peripheral artery disease (PAD) in the superficial femoral artery (SFA).

August 24, 2009 – Prescient Medical Inc. said today it received European CE mark clearance to commercialize its vProtect Luminal Shield Stent System. The device is now approved for use in improving coronary artery luminal diameter in patients with symptomatic ischemic heart disease.

August 21, 2009 - The final definition of the “meaningful use” of electronic health records that will be used to determine eligibility for incentive payments under the economic stimulus program will not be available until the middle or end of spring 2010, stated David Blumenthal, M.D., national coordinator for health information technology, in a press conference held Aug. 20.

August 21, 2009 - World Heart Corp. said today it received FDA conditional approval to begin a bridge-to-transplant (BTT) study of the Levacor Ventricular Assist Device (VAD) at 10 U.S. centers.

August 21, 2009 – The Cardiovascular Rearch Foundation, the sponsor of the Transcatheter Cardiovascular Therapeutics (TCT) symposium, will feature a series of featured clinical trials in addition to the late-breaking clinical trials at TCT 2009 in San Francisco.

August 20, 2009 - The White House announced today it will spend $1.2 billion in federal grants for electronic health records (EHR) systems, marking the first wave of funding in a series of HITECH priority grant programs, laying the groundwork for meaningful use of EHRs.