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BioSig to Host Conference Call on December 21, 2021

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BioSig Technologies (Nasdaq: BSGM) announced a conference call scheduled for December 21, 2021, at 2 PM ET to discuss its innovative signal processing platform aimed at improving ECG and intra-cardiac signal fidelity. The call will be accessible via U.S. toll-free and international numbers. The PURE EP (tm) System, BioSig's FDA-cleared device, has shown a 75% improvement in signal quality in clinical studies. With increasing cases of atrial fibrillation, the company aims to enhance cardiac care efficiency. A webcast replay will be available following the call.

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Westport, CT, Dec. 13, 2021 (GLOBE NEWSWIRE) -- BioSig Technologies, Inc. (Nasdaq: BSGM) ("BioSig" or the "Company"), a medical technology company commercializing an innovative signal processing platform designed to improve signal fidelity and uncover the full range of ECG and intra-cardiac signals, today announced that it would host a conference call on Tuesday, December 21, 2021, at 2 PM ET.

Conference Call Details
Date: Tuesday, December 21, 2021
Time: 2:00 PM Eastern Time (ET)
Dial-in number for US callers (toll-free): 877-407-8293
Dial-in number for U.S. and international callers (toll): +1 201-689-8349

To join the conference call online, please click here:
BioSig Webcast

A webcast replay will be available two hours after the event’s conclusion and archived for six months.

The PURE EP (tm) is an FDA 510(k) cleared non-invasive class II device that aims to drive procedural efficiency and efficacy in cardiac electrophysiology. Clinical data acquired by the PURE EP (tm) System in a multi-center study at Texas Cardiac Arrhythmia Institute at St. David’s Medical Center, Mayo Clinic Jacksonville, and Massachusetts General Hospital was recently published in the Journal of Cardiovascular Electrophysiology and is available electronically with open access via the Wiley Online Library. Study results showed 93% consensus across the blinded reviewers with a 75% overall improvement in intracardiac signal quality and confidence in interpreting PURE EP (tm) signals over conventional sources.

One in 18 Americans suffers from a cardiac arrhythmia. Atrial fibrillation is the most common arrhythmia type, affecting over 33 million people worldwide, including over 6 million in the U.S. The number of people suffering from atrial fibrillation is expected to reach 8-12 million by 20501. According to the Centers for Disease Control and Prevention (CDC), atrial fibrillation causes more than 750,000 hospitalizations in the U.S. each year, resulting in approximately $6 billion in healthcare spending annually2.

About BioSig Technologies
BioSig Technologies is a medical technology company commercializing a proprietary biomedical signal processing platform designed to improve signal fidelity and uncover the full range of ECG and intra-cardiac signals. (www.biosig.com).

The Company’s first product, PURE EP (tm) System is a computerized system intended for acquiring, digitizing, amplifying, filtering, measuring and calculating, displaying, recording and storing of electrocardiographic and intracardiac signals for patients undergoing electrophysiology (EP) procedures in an EP laboratory. To date, 73 physicians have completed over 1750 patient cases with the PURE EP (tm) system. The Company is in a focused commercial launch of the PURE EP (tm) System in the NortheastTexas, and Florida. The technology is regularly used in some of the country’s highest-ranked hospitals, including St. David’s Medical Center in Austin, TX, Mayo Clinic campuses in Florida, Minnesota, and Arizona, and University of Pennsylvania in Philadelphia, PA.

Forward-looking Statements
This press release contains “forward-looking statements.” Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential” or similar words. Forward- looking statements are not guarantees of future performance, are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company’s control, and cannot be predicted or quantified and consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation, risks and uncertainties associated with (i) the geographic, social and economic impact of COVID-19 on our ability to conduct our business and raise capital in the future when needed, (ii) our inability to manufacture our products and product candidates on a commercial scale on our own, or in collaboration with third parties; (iii) difficulties in obtaining financing on commercially reasonable terms; (iv) changes in the size and nature of our competition; (v) loss of one or more key executives or scientists; and (vi) difficulties in securing regulatory approval to market our products and product candidates. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Investors and security holders are urged to read these documents free of charge on the SEC’s website at http://www.sec.gov. The Company assumes no obligation to publicly update or revise its forward-looking statements as a result of new information, future events or otherwise. 




1 Top 10 Things You should Know About Heart Rhythm; Scripps Health.

2 Managing Atrial Fibrillation; Lisa Eramom MA, Medical Economics Journal, February 25, 2019, Volume 96, Issue 4



FAQ

What is the date and time of BioSig Technologies' conference call?

The conference call is scheduled for December 21, 2021, at 2 PM ET.

How can I join the BioSig Technologies conference call?

You can join the call via U.S. toll-free number 877-407-8293 or international number +1 201-689-8349.

What is the PURE EP (tm) System by BioSig Technologies?

The PURE EP (tm) System is an FDA-cleared device designed to enhance signal fidelity in cardiac procedures.

What were the clinical results of the PURE EP (tm) System?

Clinical studies showed a 75% improvement in intracardiac signal quality and a 93% consensus among blinded reviewers.

Why is atrial fibrillation a concern in the U.S.?

Atrial fibrillation affects over 6 million Americans and is projected to increase significantly by 2050.

BioSig Technologies, Inc.

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