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Nemaura Medical Inc. Receives Positive Nasdaq Listing Decision

Nemaura Medical Inc. Receives Positive Nasdaq Listing Decision

Nemaura Medical Inc. 在纳斯达克获得积极的上市决定
Nemaura Medical ·  2023/12/13 00:00
December 13, 2023
2023年12月13日

Nemaura Medical Inc. Receives Positive Nasdaq Listing Decision

Nemaura Medical Inc. 在纳斯达克获得积极的上市决定

Loughborough, UK, Dec. 13, 2023 (GLOBE NEWSWIRE) — Nemaura Medical Inc. (NASDAQ: NMRD) ("Nemaura Medical" or the "Company"), developer of a daily wear non-invasive glucose sensor, and digital healthcare programs is pleased to announce that the Nasdaq Hearings Panel granted the Company's request for continued listing pursuant to an exception, including certain interim milestones, that ultimately expires on April 1st, 2024, to evidence compliance with all applicable criteria for continued listing on The Nasdaq Capital Market.

英国拉夫堡,2023年12月13日(GLOBE NEWSWIRE)——日用非侵入性葡萄糖传感器和数字医疗项目开发商Nemaura Medical Inc.(纳斯达克股票代码:NMRD)(“Nemaura Medical” 或 “公司”)欣然宣布,纳斯达克听证会小组根据一项例外情况(包括某些临时里程碑)批准了该公司继续上市的请求,该请求最终将于4月1日到期st,2024年,以证明遵守了继续在纳斯达克资本市场上市的所有适用标准。

The Company plans to continue with its commercial endeavours while pursuing its plans to ensure timely compliance with the terms of the Nasdaq Hearing Panel's decision.

该公司计划继续开展商业活动,同时推行其计划,确保及时遵守纳斯达克听证会决定的条款。


About Nemaura Medical, Inc.


关于 Nemaura Medical, Inc.

Nemaura Medical, Inc. is a medical technology company developing and wearable diagnostic devices. The company is currently commercializing sugarBEAT and proBEAT. sugarBEAT, a CE mark approved Class IIb medical device, is a non-invasive and flexible continuous glucose monitor (CGM) providing actionable insights derived from real time glucose measurements and daily glucose trend data, which may help people with diabetes and pre-diabetes to better manage, reverse, and prevent the onset of diabetes. Nemaura Medical has submitted a proposal for a Modular PMA (Premarket Approval Application) application for sugarBEAT to the U.S. FDA, for its generation II, 24 hour sensor. proBEAT is a non-regulated version of sugarBEAT which combines non-invasive glucose data processed using artificial intelligence and a digital healthcare subscription service as a general wellness product as part of its BEATdiabetes program.

Nemaura Medical, Inc. 是一家开发可穿戴诊断设备的医疗技术公司。该公司目前正在将 SugarBeat 商业化 和 ProBeat. SugarBe是一款获得 CE 标志批准的 IiB 类医疗设备,是一种非侵入性、灵活的连续血糖监测仪 (CGM),可提供从实时血糖测量值和每日血糖趋势数据中得出的切实可行的见解,可以帮助糖尿病和糖尿病前期患者更好地管理、逆转和预防糖尿病的发作。Nemaura Medical 已提交了 SugarBeat 模块化 PMA(上市前批准申请)申请提案 致美国食品药品管理局的第二代 24 小时传感器。ProBeat 是 SugarBeat 的非监管版本,它结合了使用人工智能处理的非侵入性葡萄糖数据和数字医疗订阅服务作为普通健康产品作为其 BEAT 的一部分糖尿病计划。

Additionally, Nemaura Medical launched a beta trial of Miboko, a metabolic health and well-being program using a non-invasive glucose sensor along with an AI mobile application that helps a user understand how certain foods and lifestyle habits can impact one's overall metabolic health and well-being. Nemaura Medical believes that up to half the population could benefit from a sensor and program that monitors metabolic health and well-being.

此外,Nemaura Medical还启动了Miboko的测试版试验,Miboko是一项新陈代谢健康和福祉计划,使用非侵入性葡萄糖传感器和人工智能移动应用程序,可帮助用户了解某些食物和生活习惯如何影响一个人的整体代谢健康和福祉。Nemaura Medical认为,多达一半的人口可以从监测新陈代谢健康和福祉的传感器和程序中受益。

The Company sits at the intersection of the global Type 2 diabetes market that is expected to reach nearly $59 billion by 2025, the $50+ billion pre-diabetic market, and the wearable health-tech sector for weight loss and wellness applications that is estimated to reach $60 billion by 2023.

该公司位于全球2型糖尿病市场(预计到2025年将达到近590亿美元)、超过500亿美元的糖尿病前期市场和用于减肥和健康应用的可穿戴健康技术领域的交汇点,预计到2023年将达到600亿美元。

For more information, please visit www.NemauraMedical.com.

欲了解更多信息,请访问 www.nemauramedical.com


Cautionary Statement Regarding Forward-Looking Statements:


关于前瞻性陈述的警示声明:

The statements in this press release that are not historical facts may constitute forward-looking statements that are based on current expectations and are subject to risks and uncertainties that could cause actual future results to differ materially from those expressed or implied by such statements. Those risks and uncertainties include, but are not limited to, the launch of proBEAT in the U.S., risks related to regulatory status and the failure of future development and preliminary marketing efforts, Nemaura Medical's ability to secure additional commercial partnering arrangements, risks and uncertainties relating to Nemaura Medical and its partners' ability to develop, market and sell proBEAT, the availability of substantial additional equity or debt capital to support its research, development and product commercialization activities, and the success of its research, development, regulatory approval, marketing and distribution plans and strategies, including those plans and strategies related to both proBEAT digital health, and sugarBEAT. There can be no assurance that the company will be able to reach a part of or any of the global market for CGM with its products/services. The U.S. Food and Drug Administration (the "FDA") reserves the right to re-evaluate its decision that proBEAT qualifies as a general wellness product should it become aware of any issues such as skin irritation or other adverse events from the device, as well as any misuse impacting patient safety, and any other reason as the FDA may see fit at its discretion to determine the product does not fit the definition of a general wellness product. These and other risks and uncertainties are identified and described in more detail in Nemaura Medical's filings with the United States Securities and Exchange Commission, including, without limitation, its Annual Report on Form 10-K for the most recently completed fiscal year, its Quarterly Reports on Form 10-Q, and its Current Reports on Form 8-K, each as may be amended from time to time. Nemaura Medical undertakes no obligation to publicly update or revise any forward-looking statements.

本新闻稿中非历史事实的陈述可能构成前瞻性陈述,这些陈述基于当前预期,存在风险和不确定性,可能导致未来的实际业绩与此类陈述所表达或暗示的结果存在重大差异。这些风险和不确定性包括但不限于 ProBeat 的发布 在美国,与监管状况相关的风险、未来开发和初步营销工作的失败、Nemaura Medical获得额外商业合作安排的能力、与Nemaura Medical及其合作伙伴开发、营销和销售ProBeat的能力相关的风险和不确定性,用于支持其研究、开发和产品商业化活动的大量额外股权或债务资本的可用性,以及其研究、开发、监管部门批准、营销和分销计划和战略的成功,包括与ProBeat两者相关的计划和战略 数字健康和 SugarBeat。无法保证该公司能够凭借其产品/服务进入CGM的部分或任何全球市场。美国食品药品监督管理局(“FDA”)保留重新评估其决定 ProBeat 的权利 如果发现任何问题,例如设备引起的皮肤刺激或其他不良事件,以及任何影响患者安全的滥用行为,以及美国食品和药物管理局可能认为合适的任何其他原因来确定该产品不符合普通健康产品的定义,则有资格作为普通健康产品。Nemaura Medical在向美国证券交易委员会提交的文件中更详细地确定和描述了这些风险和不确定性,包括但不限于其最近完成的财年的10-K表年度报告、10-Q表的季度报告和8-K表的最新报告,每份报告都可能不时修改。Nemaura Medical没有义务公开更新或修改任何前瞻性陈述。


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