 Investors  PhysioSign's device addresses the No. 1 Cause of Death - Heart Disease, addresses the No. 1 Healthcare Problem - Cost, and applies the No. 1 Healthcare Technology - AI. PhysioSign is looking to raise $25-30 million in the U.S. Please see our 10 minute pitch deck here. ________________________________________________________________________ Use Of Funds Regulatory - Create regulatory staff and obtain device approvals in the U.S. and Europe. As shown above, PhysioSign's AI-EKG-ECG's compatibility with and use of the standard PQRST waveform should make regulatory approval straightforward. Sales and Marketing - Hire sales and marketing staff and purchase devices for sale in US and Europe. Market and sell clinical devices in the US and Europe. R&D - Fund continued research and development. ________________________________________________________________________ Competitors Conventional EKG See the top five conventional EKG manufacturers here. AI Post-processing of conventional EKG Mayo Clinic has used AI to detect heart failure from a conventional EKG signal also Mayo Clinic has used AI for ECG screening for asymptomatic left ventricular dysfunction also Mayo Clinic using AI with EKG can detect a form of heart disease, research shows also New AI-assisted ECG offers early heart disease detection also Artificial Intelligence From ECGs May ID Asymptomatic LV Dysfunction also Artificial Intelligence-Enabled ECG May Screen for Asymptomatic LV Dysfunction Cardiologs has used AI to detect arrhythmias from a conventional EKG signal also Cardiologs raised $6.5 million in 2017 also How AI Can Analyze ECG Data Faster also FDA 510k summary (2017) also 2016 French Study Stanford University team has used AI to detect irregular heat beats from a conventional EKG signal also Cardiologist-Level Arrhythmia Detection With Convolutional Neural Networks also Machine Learning Algorithm Outperforms Cardiologists Reading EKGs AliveCor's AI software for EKG rhythms gets market OK also FDA 510k summary (4/2019) FDA 510k Summary (11/2017) ACME FDA 510k Compared to GE and Philips devices. ________________________________________________________________________ Contact |