Global WholeHealth Partners Corp (OTC: GWHP) through this agreement is funded for growth, sales, and expansion. Per the terms of the EMC2 Purchase Agreement, we may direct EMC2 to purchase up to $100,000,000 worth of shares of our common stock under our agreement over a 36-month period, generally in amounts up to 100,000 shares of our common stock, which may be increased to up to 2,000,000 shares of our common stock depending on the market price of our common stock at the time of sale and subject to a maximum commitment by EMC2 of $500,000 per regular purchase per day. The total amount of shares to be sold through the EMC2 agreement is up to 8,578,177 shares of common stock.
Global WholeHealth Partners Corp. (OTC:GWHP) provides cutting edge technology using In-vitro Diagnostic (IVD) Real-Time PCR Machines for detection of SARS-CoV-2 IgM/IgG antibodies in human serum, plasma, or whole blood. It has led the fight against vector borne terminal diseases such as Ebola, ZIKA, Dengue, Malaria, Influenza and Tuberculosis, Corona Viruses, and among other vector borne diseases with an FDA Certificate of Exportability (2260-11-2019). The company was founded on March 7, 2013 and is headquartered in San Clemente, CA.
GWHP develops, manufactures, and markets in vitro diagnostic (IVD) tests for OTC, or consumer-use as well as professional rapid diagnostic point-of-care (POC) test kits for hospitals, physicians’ offices, and medical clinics in the US and abroad. Currently, the Company has 70 products FDA approved and many are approved for OTC use, and 29 POC products approved by the FDA CLIA WAIVED.
Call or email about special prices for this announcement on all the tests.
The Company is not making any express or implied claims that its product has the ability to eliminate, cure or contain the Covid-19 (or SARS-2 Coronavirus) at this time.
Name: Charles Strongo,
CEO, Global WholeHealth Partners Corp.
Email: Sales@gwhpcorp.com Phone for Sales: 877-568-4947
This press release contains “forward-looking statements.” 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) market acceptance of our existing and new products, (ii) negative clinical trial results or lengthy product delays in key markets, (iii) an inability to secure regulatory approvals for the sale of our products, (iv) intense competition in the medical device industry from much larger, multinational companies, (v) product liability claims, (vi) product malfunctions, (vii) our limited manufacturing capabilities and reliance on subcontractors for assistance, (viii) insufficient or inadequate reimbursement by governmental and other third party payers for our products, (ix) our efforts to successfully obtain and maintain intellectual property protection covering our products, which may not be successful, (x) legislative or regulatory reform of the healthcare system in both the U.S. and foreign jurisdictions, (xi) our reliance on single suppliers for certain product components, (xii) the fact that we will need to raise additional capital to meet our business requirements in the future and that such capital raising may be costly, dilutive or difficult to obtain and (xiii) the fact that we conduct business in multiple foreign jurisdictions, exposing us to foreign currency exchange rate fluctuations, logistical and communications challenges, burdens and costs of compliance with foreign laws and political and economic instability in each jurisdiction. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company’s filings with the Securities and Exchange Commission (SEC), including the Company’s Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Investors and security holders are urged to read these documents free of charge on the SEC’s web site 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.
BioRegenx Announces Investor Update
CEO, William Resides announces that as of July 1st, 2022, BioRegenx has moved from due diligence to a binding letter of intent to merge with a public company. These steps also include drafting of the definitive agreement for final merger.
As part of the merger activity, BioRegenx has hired Dan Cortes, CPA as its CFO. This decision was made in part to Dan’s track record as an experienced corporate financial CFO with more than 20 years of progressive experience in financial operations and taxation with both private and public organizations ranging from startups to those with hundreds of millions in revenue.
Microvascular Health Solutions Developments
After 18-months of research and development, followed by rigorous testing, Microvascular Health Solutions has approved final production of a new camera capable of taking six times more video images gathered from under the tongue. The new patent-pending camera is called CapiVision™. The components for 1,000 CapiVision cameras have been ordered and production has begun with delivery expected late Q3, early Q4.
Along with development of the new CapiVision camera, the MVHS team has completed development of the 5.2.7 version of the GlycoCheck software and new video acquisition software that quality-check videos recorded by the CapiVision camera. Test results will be calculated on a new high-powered custom laptop computer capable of quickly processing results.
The next stage of software development is for the processing of the GlycoCheck video images to be transmitted to the cloud for calculation and storage of the MicroVascular Health Score™ as a Software as a Service (SaaS). This will run on the Microsoft™ Azure Platform. The development is ongoing with our technology team in the Netherlands and the first version is expected to be released Q4, 2022.
Our plan is to bring the GlycoCheck system now being used in over 140 academic research hospitals studying a wide range of conditions and diseases, into a much-anticipated targeted system for medical and professional office use that generates a personalized MicroVascular Health Report for individual patients. To support medical and professional office use, we have created a series of 19 GlycoCheck System training modules, with more coming in the future. Once a provider views the videos and takes a test for each module, and a passing score is completed for all modules, a certificate of completion is issued. The training platform is hosted by the Boston BioLife Academy, a leading training, CME credit, and in-person events company for MD’s and Practitioners across the U.S.
There are now 90 peer-reviewed published studies using GlycoCheck in major medical journals that have researched how diseases and conditions are linked to a decline in endothelial glycocalyx function and a leaky, compromised microvascular system. Those studies range from health issues like sepsis, COVID-19, kidney disease, heart disease, cerebrovascular events, psoriasis, and many more. View the entire list at https://glycocheck.com/research-and-studies/#published. If you have a specific disease or condition you wish to read more about, type the name in the “Search” function to narrow the studies down to your specific interest.
BioRegenx’ wholly owned subsidiary, NuLife Sciences announces the release of its latest product and service, TruEpigenetics via the Apple Store and Google Play. TruEpigenetics has launched on www.NuLifeSciences.com/TruEpigenetics. Now, you can discover your biological age and take control of your genetic health with a simple saliva test. The TruEpigenetics Practitioner and Patient on-boarding portal is expected for release in late Q3.
Referral Link Development for Sales Tracking
Currently, we are in the in final phase of testing of NuLife Sciences’ Hybrid-Direct Sales and Practitioner referral link program. This will allow all BioRegenx’ subsidiaries to utilize referral links, commission tracking, and account on-boarding for both our professional clients’ practices as well as their patients.
Endocalyx Pro™ Double-Blind Placebo Studies
Double-blind placebo studies on the effectiveness of Endocalyx Pro have been running since 2015. In-depth studies take years to complete, and we are just now seeing the results from those studies. These studies are in cell cultures, animal trials, as well as human studies. These studies are on the following health conditions and diseases:
Additional studies currently being written and in the approval process will be devoted to these conditions:
Emergency Room Admissions
Arterial Plaque Development
Review these studies and more at https://microvascular.com/endocalyx-pro-studies
BioRegenx, Inc., (https://bioregenx.com/) a holding company, consists of Microvascular Health Solutions, LLC, My Body Rx, LLC, and NuLife Sciences, Inc. BioRegenx and its subsidiaries combine the patented intellectual property of the breakthrough GlycoCheck medical testing device, the patented nutraceutical Endocalyx Pro, additional synergistic dietary supplement products sold under the My Body Rx brand, and a customer base of medical professionals and brand partners throughout North America.
Microvascular Health Solutions (MVHS) is a research and product development, sales, education, and marketing company that has developed the patented and clinically tested Endocalyx Pro™ dietary supplement to improve the health of the endothelial glycocalyx. In addition, MVHS manufactures, exclusively sells, and distributes the patented GlycoCheck™ software and Class 1 medical device that measures and analyzes the endothelial glycocalyx, a transparent lining inside all blood vessels.
My Body Rx™ is a manufacturing, sales and product development company that produces dietary supplements that complement and work synergistically with the patented and clinically tested Endocalyx Pro™ product to support and improve healthy aging and increase longevity.
NuLife Sciences, Inc. is a marketing and distribution company whose mission is to harness advanced technologies to redefine health and longevity. This is achieved by increasing understanding of the biology that controls lifespan and anti-aging in the human body. NuLife exclusively markets the My Body Rx™ supplement line. NuLife will also distribute GlycoCheck™, TruEpigenetics, and additional new products currently under consideration.
This press release contains forward-looking information within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), including statements regarding potential sales, the success of the company’s business, as well as statements that include the word believe or similar expressions. Such forward-looking statements involve known and unknown risks, uncertainties, and other factors that may cause the actual results, performance, or achievements of BioRegenx, Inc. to differ materially from those implied or expressed by such forward-looking statements. This press release speaks as of the date first set forth above, and BioRegenx, Inc. assumes no responsibility to update the information included herein for events occurring after the date hereof. Actual results could differ materially from those anticipated due to factors such as the lack of capital, timely development of products, inability to deliver products when ordered, inability of potential customers to pay for ordered products, and political and economic risks inherent in international trade
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WynCore Offers Complete WMS Modifications to Enhance your Manhattan Software
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We offer you a full host of services including: design and implementation, QA Testing, customized maintenance and support, along with training. Your warehouse management software could use small adjustments or need a major redesign where training and support are required. Our flexible lineup of services allows us to quickly find the best solution for you. In addition, we are proud to note that WynCore developers and project management teams are experts in both Agile and Waterfall methodologies and well versed in DEV-OPS.
We are the trusted and preferred choice for Manhattan software WMS modifications needed for the challenges of today and in the future. Our developers can quickly design a customized set of services to assist you in operating your warehouse flawlessly. From minor tweaks and adjustments to your WMS or a complete overhaul, WynCore professionals craft a customized plan to suit your timeline and budget.
Our support to you does not stop at the end of your WMS customization services. WynCore project management and global support teams provide assistance whenever you need it 24/7 to help minimize disruptions with any arising issue, even after a modification or upgrade is completed.
WynCore provides the plan, implementation and support especially for you. A seamless integration, modification and upgrade or total overhaul that fits your bottom line can be in your future. Reach out today and speak with our software developers about your warehouse management software upgrade services and customization needs by calling us at 866-996-2673.