Santa Monica, CA, Nov. 28, 2018 (GLOBE NEWSWIRE) -- BioSig Technologies, Inc. (NASDAQ: BSGM), a medical device company developing a proprietary biomedical signal processing platform designed to address an unmet technology need for the $4.6 billion electrophysiology (EP) marketplace, today announced that the Company formed a Clinical Advisory Board to complement existing scientific relationships with the nationwide key opinion leaders built during the R&D phase of product development.
The goal of the newly formed Board is to advise the Company on a range of aspects related to commercialization of BioSig’s novel signal acquisition and processing technology, PURE EP(tm) System. Physicians from 17 leading medical centers in the United States will be gathering for the Board’s first meeting on November 30, 2018. The agenda will include focused consultations on the human clinical data collection, commercial strategy for PURE EP(tm) System and potential clinical benefits of new technologies in the R&D pipeline.
“Our technology has been developed together with some of the most respected key opinion leaders in the electrophysiology industry. As we progress towards full commercial launch of our PURE EP(tm) System, it is essential to engage a wider group of talented physicians who can strengthen our product and launch plan. We are pleased that so many leading electrophysiologists agreed to dedicate their valuable time and provide input to help us better address unmet clinical needs in this very complex area of arrhythmia treatments,” commented Kenneth L. Londoner, Chairman and CEO of BioSig Technologies, Inc.
BioSig received FDA 510(k) clearance for its first product, PURE EP(tm) System on August 8, 2018. The Company began trading on the Nasdaq Capital Markets on September 21, 2018 under the ticker symbol BSGM.
About BioSig Technologies
BioSig Technologies is a medical technology company developing a proprietary biomedical signal processing platform designed to improve the electrophysiology (EP) marketplace (www.biosigtech.com). Led by a proven management team and a veteran, independent Board of Directors, Los Angeles-based BioSig Technologies is preparing to commercialize its PURE EP™ System. The technology has been developed to address an unmet need in a large and growing market.
The Company’s first product, PURE EP™ System, is a novel cardiac signal acquisition and display system which is engineered to assist electrophysiologists in clinical decision- making during procedures to diagnose and treat patients with abnormal heart rates and rhythms. BioSig’s main goal is to deliver technology to improve upon catheter ablation treatments for the prevalent and potentially deadly arrhythmias, Atrial Fibrillation and Ventricular Tachycardia. BioSig has partnered with Minnetronix on technology development and has received FDA 510(k) clearance for the PURE EP™ System in August 2018.
Forward-looking Statements
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