BioSig Announces Reduction of its Workforce
February 20 2024 - 10:00AM
-- BioSig Technologies, Inc. (NASDAQ: BSGM) ("BioSig" or the
"Company"), a medical technology company, today announced that it
has terminated a significant number of its employees and expects to
substantially reduce business operations.
About BioSig Technologies, Inc.
BioSig Technologies is a medical technology company.
The Company's product, the PURE EP™ Platform, an FDA 510(k)
cleared non-invasive class II device, provides superior, real-time
signal visualization, allowing physicians to perform highly
targeted cardiac ablation procedures with increased procedural
efficiency and efficacy.
An estimated 14.4 million Americans suffer from cardiac
arrhythmias, and the global EP market is projected to reach $16B in
2028 with an 11.2% growth rate.1
Forward-Looking Statements
This press release contains "forward-looking statements" within the
meaning of the Private Securities Litigation Reform Act of 1995.
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) BioSig’s ability to regain
compliance with and meet the continued listing requirements of the
Nasdaq Capital Market to maintain listing of its common stock; (ii)
the geographic, social, and economic impact of pandemics or
worldwide health issues on BioSig’s ability to conduct its business
and raise capital in the future when needed; (iii) BioSig’s
inability to manufacture its products and product candidates on a
commercial scale on its own, or in collaboration with third
parties; (iv) difficulties in obtaining financing on commercially
reasonable terms; (v) changes in the size and nature of BioSig’s
competition; (vi) loss of one or more key executives or scientists;
(vii) BioSig’s cost reduction plan and associated workforce
reduction or other cost-saving measures not reaching the targeted
reduction of cash burn by 50%; and (viii) difficulties in securing
regulatory approval to market BioSig’s products and product
candidates. For a discussion of other risks and uncertainties, and
other important factors, any of which could cause BioSig’s actual
results to differ from those contained in forward-looking
statements, see Biosig’s filings with the Securities and Exchange
Commission (“SEC”), including the section titled “Risk Factors” in
BioSig’s Quarterly Report on Form 10-Q, filed with the SEC on
November 14, 2023. 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, except as required by
law.
1 Cardiac Ablation Market. (2022, December). Global
Market Insights.
https://www.gminsights.com/industry-analysis/cardiac-ablation
BioSig Technologies, Inc.
55 Greens Farms
Westport, CT 06880
203-409-5444, x133
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