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REDWOOD CITY, Calif., Mar. 19, 2019 (GLOBE NEWSWIRE) — Biotricity Inc. (OTCQB:BTCY), a medical diagnostic and consumer healthcare technology company, is pleased to announce further buildout of its R&D team, with the engagement of the Biomedical Engineering Department at the University of Calgary. The expanded team will include a Biomedical Engineering (BME) fellow under Dr. Ferber, Director of Biomedical Engineering’s Human Performance Laboratory, who will explore and develop effective representations of both fetal/maternal heart rate variability (HRV) and electro-hysterography (labor contraction monitoring) in pregnancy. Dr. Ferber and the BME Department have extensive experience working with industry leaders, including Garmin and Nike, on practical applications.

Dr. Ferber and the BME fellow will use clinical data gathered from expectant mothers in active labor, supporting their analysis with U of C’s Engineering faculty’s recognized expertise in signal processing. In conjunction with the U of C Cumming School of Medicine, the monitoring systems will be optimized and clinically validated, building on both the initial ICU based testing of the Bioflux prototype and commonly accepted heart-rate based algorithms used to assess babies during labor. The Bioflux prototype has already identified a fundamental and easily demonstrated difference in the relationship between heart rate and HRV, in sickness and in wellness. Biotricity will also facilitate all parties in their investigation to determine what role artificial intelligence can play in assisting with clinical interpretation.

The Company looks forward to the development of two new product lines with a clinical and consumer model, similar to the Bioflux and future Biolife product dynamic. Combining Biotricity’s high-fidelity electrically based monitoring with actual clinical data and BME’s proven engineering expertise, the U of C/Biotricity program is expected to produce systems to facilitate mobile monitoring for both mothers and babies prior to and during delivery. The expertise in data-processing efficiency and effective information display design will also be applicable to the Company’s ongoing program using HRV monitoring to track wellness and sickness in both ambulatory consumers and in patients under care across a broad range of medical and surgical indications.

Dr. David Liepert, QA/QI and Safety Lead and Director for the University of Calgary Cumming School of Medicine Department of Anesthesia commented, “Biotricity CEO Waqaas Al-Siddiq has created an unprecedented developmental partnership between Calgary University’s Schools of Medicine and Engineering. As a medical educator, I feel that the opportunity for both residents and fellows to work with Biotricity’s wet-lead and dry-lead systems, machine learning, and AI is foundational. As a Quality and Safety Director, I believe that providing higher quality information and guidance with less discomfort and risk is a game-changer for the healthcare industry.”

Appropriate pre-habilitation and post-surgical rehabilitation has been shown to save up to $2,000 dollars per patient and per surgery. Today, 89 percent of laboring patients in North America currently receive electronic fetal monitoring using either lower fidelity and less precise sound-based electrodes or higher fidelity fetal scalp electrodes. Labor contraction and pressure monitoring inserted through the vagina is used in approximately 15 percent of deliveries. Both electrode monitoring and trans-vaginal intrauterine pressure monitoring are invasive techniques that introduce possible trauma, infection and patient discomfort. Remote fetal/maternal monitoring has been shown to lead to better prenatal health outcomes by identifying certain high-risk conditions such as pre-eclampsia earlier and with more precision, providing timely interventions to resolve high-risk conditions and enabling a more convenient delivery of prenatal care. Long term, it will facilitate safer and more comfortable labor room care with reduced costs, making unforeseeable risks less costly and more predictable, manageable and potentially preventable.

Biotricity seeks to facilitate the development of future medical devices that are easy to utilize in either the physician’s office or the patient’s home as well as in acute-care settings. These medical-grade wearable devices are comfortable, small and can offer precise remote data collection and more responsive care.

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About Biotricity Inc.

Biotricity is a modern medical technology company focused on delivering innovative, remote biometric monitoring solutions to the medical and consumer markets, including diagnostic and post-diagnostic solutions for chronic conditions and lifestyle improvement. Biotricity’s R&D continues to focus on the preventative healthcare market, with a vision of putting health management into the hands of the individual. The company aims to support the self-management of critical and chronic conditions with the use of innovative solutions to ease the growing burden on the healthcare system. To learn more, visit

Important Cautions Regarding Forward-Looking Statements

Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements. Forward-looking statements, which involve assumptions and describe our future plans, strategies, and expectations, are generally identifiable by use of the words “may,” “should,” “would,” “will,” “could,” “scheduled,” “expect,” “anticipate,” “estimate,” “believe,” “intend,” “seek,” or “project” or the negative of these words or other variations on these words or comparable terminology. Forward-looking statements may include, without limitation, statements regarding (i) the plans and objectives of management for future operations, including plans or objectives relating to the design, development and commercialization of Bioflux or any of the Company’s other proposed products or services, (ii) a projection of income (including income/loss), earnings (including earnings/loss) per share, capital expenditures, dividends, capital structure or other financial items, (iii) the Company’s future financial performance, (iv) the regulatory regime in which the Company operates or intends to operate and (v) the assumptions underlying or relating to any statement described in points (i), (ii), (iii) or (iv) above. Such forward-looking statements are not meant to predict or guarantee actual results, performance, events or circumstances and may not be realized because they are based upon the Company’s current projections, plans, objectives, beliefs, expectations, estimates and assumptions and are subject to a number of risks and uncertainties and other influences, many of which the Company has no control over. Actual results and the timing of certain events and circumstances may differ materially from those described by the forward-looking statements as a result of these risks and uncertainties. Factors that may influence or contribute to the inaccuracy of the forward-looking statements or cause actual results to differ materially from expected or desired results may include, without limitation, the Company’s inability to obtain additional financing, the significant length of time and resources associated with the development of its products and related insufficient cash flows and resulting illiquidity, the Company’s inability to expand the Company’s business, significant government regulation of medical devices and the healthcare industry, lack of product diversification, existing or increased competition, results of arbitration and litigation, stock volatility and illiquidity, and the Company’s failure to implement the Company’s business plans or strategies. These and other factors are identified and described in more detail in the Company’s filings with the SEC. The Company assumes no obligation to update any forward-looking statements in order to reflect any event or circumstance that may arise after the date of this release.


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