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NovioSense Announces Positive Clinical Trial Results of Tear Glucose Measurement Technology
NovioSense has demonstrated the measurement of tear glucose in diabetic patients and a close correlation to blood glucose with clinically relevant accuracy. A second, 24-patient study, to validate the use of the new glucose sensor in type 1...
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GO2SLEEP: AI-Powered Device for Restful Sleep
The Go2Sleep Home Sleep Test is a revolutionary device on monitoring and improving your sleep quality. It elevates comfort while maintaining almost the same detecting accuracy of a pulse oximeter, but with a lot more key information. The precise...
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2-Day In-Person Seminar: Medical Device Single Audit Program Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients...
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Ceribell Announces Completion of $35 Million Series B Financing
Proceeds will be used to expand commercialization of its innovative Rapid Response EEG System to improve the diagnosis and treatment of patients at risk for seizures MOUNTAIN VIEW – September 25, 2018 – Ceribell, Inc. announced today that the...
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Inside Hologic’s Evolving Definition of Women’s Healthcare
Hologic (NSDQ:HOLX), known in the medtech industry for its mammography and diagnostics devices, is rethinking what it means to be a women’s healthcare company. The 6,000-person company wants to expand its reach to include products that care...
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Risk Management in Medical Devices Industry: a 2-Day In-Person Seminar
Risk management is a mandatory and necessary process during the entire device life. Not only will it help to design and maintain devices efficiently, but it also ensures that the device will be as safe as possible and prevents harms to patients,...
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Vendor and Supplier Qualification Program for FDA Regulated Industries
The FDA regulates manufacturers of medical products such as devices, pharmaceuticals, tissue products, and biologics. However, the regulations don’t usually extent to suppliers. Instead, the FDA expects the medical product manufacturer to...
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Two-Day Interactive Course on In-Vitro Diagnostics Regulations
In-vitro Diagnostics (IVD) products provide critical information on patient’s health condition, based on which the healthcare provider develops and administers treatment plan. Although IVDs are medical devices, they are regulated under a separate...
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How Cloud Faxing Improves Productivity in Healthcare
The humble fax machine has been a regular fixture within healthcare offices for as long as most of us care to remember. Even in 2018, with so much modern technology at our disposal, fax machines continue to dominate an otherwise rapidly evolving...
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