Monthly Archives: June 2019

Margaret Lake Diamonds and Cache Exploration Receive Shareholder Approval for Kiyuk Lake Gold Property Transaction

VANCOUVER, BC / ACCESSWIRE / June 25, 2019 / Margaret Lake Diamonds Inc. (TSX.V: DIA / FSE: M85) (“Margaret Lake” or the “Company”) is pleased to report that Cache Exploration Inc. (“Cache”) (TSX.V: CAY) shareholders have approved the proposed acquisition (the “Transaction”) in which the Company will acquire up to an 80% interest in the Kiyuk
Lake Gold Property
(“Kiyuk Lake” or the “Property”) located in southern Nunavut. The Companies will be filing a NI 43-101 technical report to support the technical disclosure of the Transaction shortly.

About the Kiyuk Lake Gold Property

The Kiyuk Lake land package consists of 70 contiguous mineral claims encompassing over 59,000 hectares and offers year-round accessibility to a 35-person base camp. Significant past exploration, beginning with Newmont Mining in 2008 and most recently Cache Exploration in 2017, has resulted in over 13,000 meters of core drilling and delineation of four mineralized zones and five additional high priority target areas that have yet to be drill tested. Mineralization has been traced across a 13-kilometer strike length and remain open in all directions. The main focus of exploration to date has been on the high-grade Rusty zone. In 2017, drilling within the Rusty zone returned broad intercepts of gold mineralization including:

8m of 26.48 g/t gold from 108m, including 2m of 92.76 g/t gold from 110m, in DDH KI17-001

38m of 1.16 g/t gold from 58m, including 8m of 3.98 g/t gold from 68m, in DDH KI17-002

122m of 1.82 g/t gold from 188m, including 15m of 3.34 g/t gold from 294m, in DDH KI17-004

249m of 1.6 g/t gold from 8.2m in DDH KI13-004 (no cut-off)

* Drill intercepts are not true width. True widths are not known at this time. See Cache Exploration Inc. press releases dated October 12, 2017 and October 26, 2017 and Prosperity Goldfields press release dated April 9, 2013. While the Company believes the historical work was performed according to best practices and the exploration data is reliable, a Qualified Person has not verified the results independently.

Figure 1. Kiyuk Lake Project Map

Qualified Person

The technical data in this news release has been reviewed and approved by Buddy Doyle, P.Geo., a Qualified Person under the provisions of National Instrument 43-101.

About Margaret Lake Diamonds Inc.

Margaret Lake Diamonds Inc. (TSX.V: DIA) is a Canadian junior mining company focused on mineral exploration in Canada’s most prolific mining districts. The Company is earning an 80% interest in the high-grade Kiyuk Lake Gold Property located in southern Nunavut and also holds interests in two diamond exploration properties in the Northwest Territories- the Margaret Lake project located adjacent to Mountain Province Diamond’s Kennady North project and close proximity to Gahcho Kué, the newest Canadian diamond mine owned by De Beers and Mountain Province Diamonds. The Company has a 60/40 joint venture with Arctic Star Exploration Corp. (TSX.V: ADD) to explore the Diagras property, which is comprised of 23 claims totaling 18,699 hectares located in the prolific Lac de Gras diamond field.

ON BEHALF OF THE BOARD OF DIRECTORS

“Jared Lazerson”
President and Chief Executive Officer
Phone: 1.604.630.2810
Web: www.margaretdiamonds.com

Forward-Looking Statements

This news release contains forward-looking information that involves various risks and uncertainties regarding future events. Such forward-looking information can include without limitation statements based on current expectations involving a number of risks and uncertainties and are not guarantees of future performance of the Company. Actual results and future events could differ materially from anticipated in such information. These and all subsequent written and oral forward-looking information are based on estimates and opinions of management on the dates they are made and expressed qualified in their entirety by this notice.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

SOURCE: Margaret Lake Diamonds Inc.

ReleaseID: 549784

EastWest Bioscience Starts Production of CBD Pet Treats for the US Market

VANCOUVER, BC / ACCESSWIRE / June 25, 2019 / EastWest Bioscience (the “Company” or “EastWest”) (TSX.V: EAST) announces that, further to its News Release on April 26th, 2019, that the Company has started production of CBD infused Chill Dog and Quick Cat for the US Market.

+CBD Chill Dog and +CBD Quick Cat will be sold through the company’s Kentucky based distribution arm, EastWest Science USA. The products are currently in production and scheduled to be available in August. EastWest is working with distributors in the US for product launch pre-orders.

“The Company views the growth estimates for CBD pet products as a significant and early trend in the CBD industry. We are speaking to several distributors and retailers who are very excited about our newest products.” Says Fanika Jovanovic Perika, Global Business Development Leader, EastWest Bioscience.

EastWest’s product development and sales strategy for pet treats in the USA will mirror the Company’s Canadian sales strategy: gain brand awareness and establish distribution relationships for broad product distribution. As it establishes relationships with various distributors to sell the Company’s unique and innovative hemp-based products, the Company is readying to expand each product to +CBD.

The Company’s “CBD Ready” formulation strategy will result in 12 niche-market pet treats products available to the US market: six hemp-based pet treats with CBD and six hemp-based pet treats without CBD, catering to all market segments. As EastWest’s hemp products become established in retail stores and distribution networks, it lowers the barrier of entry for the Company’s CBD infused products.

“As demand of Hemp and CBD products continues to grow, EastWest is excited to be making headway with our Natural Pet Science +CBD line. Pet Care is one of the hottest trending segments of the CBD industry.” States Rodney Gelineau, CEO of EastWest Bioscience.

About EastWest Bioscience Group

EastWest Bioscience is a vertically integrated wellness company with the infrastructure to become a global giant in the Hemp & CBD consumer health market. Since it was founded in 2016, EastWest continues to grow as a high-quality producer, manufacturer and distributor of multiple lines of premium health and hemp products. EastWest currently has more than 200+ NPN’s in its stable of products.

EastWest’s Hemp consumer product lines are divided into four distinct brands: 1) Natural Advancement – natural biopharmaceutical health supplements; 2) Earth’s Menu – all-natural hemp superfoods; 3) Natural Pet Science – pet food and pet supplements; and 4) ChanvreHemp – all-natural health and beauty products.

In Canada, EastWest has a 34,000 Sq. Ft, Health Canada-licensed, GMP (Good Manufacturing Practices) – certified manufacturing facility and produces premium nutraceutical brands, offering natural products for a preventive care lifestyle. EastWest and Benchmark Botanicals (BBT-CSE) also have a Joint Venture Intent to accelerate acquisition of Processor, Analytical and Research and Development licenses under the Cannabis Act in EastWest’s Penticton facility. These three classes of the Cannabis Act license will allow Benchmark and EastWest to build out an extensive extraction, laboratory, and research facility at EastWest’s Health Canada Certified facility.

In the USA, EastWest USA has a Joint Venture with Azema Sciences, securing for EastWest first rights on Azema’s output of bulk CBD and finished CBD products manufactured, and which are ready for sale in the USA and globally. EastWest Science USA (“EastWest USA”), EastWest’s US operating division, will be the preferred distributor for Azema’s finished goods. These finished products will include CBD creams, tinctures and salves which are products not currently in EastWest’s catalogue. Additionally, EastWest will have first right of refusal to all potential opportunities relating to Azema’s Kentucky based CBD processing facility. EastWest currently has TSX Approval for sale of its consumer products in 21 US States.

EastWest’s international expansion continues with reach into important key markets in New Zealand, Australia, and Asia through a distributor agreement with New Zealand Hemp Brokers. Headquartered in Rotorua, New Zealand, NZ Hemp Brokers have quickly grown to become one of the country’s most trusted industrial hemp wholesalers, and New Zealand’s only import/export broker specialising in hemp products. NZ Hemp Brokers is licensed by the NZ Ministry of Health to grow, trade in and process industrial hemp, are registered brokers and certified in hemp medicine by the NZ Hemp Foundation.

ON BEHALF OF THE BOARD OF DIRECTORS
EASTWEST BIOSCIENCE GROUP

“Rodney Gelineau”
Co-Founder, Chief Executive Officer and Director

TSXV – Symbol: EAST

Company Website: www.eastwestbioscience.com
Contact: Nicholas Vincent – Investor Relations on 1-800-409-1930 or investors@eastwestscience.com.

NEITHER THE TSX VENTURE EXCHANGE NOR ITS REGULATION SERVICES PROVIDER (AS THAT TERM IS DEFINED IN THE POLICIES OF THE TSX VENTURE EXCHANGE) ACCEPTS RESPONSIBILITY FOR THE ADEQUACY OR ACCURACY OF THIS RELEASE.

CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING INFORMATION: This news release includes certain “forward-looking statements” under applicable Canadian securities legislation. Forward-looking statements include, but are not limited to, statements with respect to the terms and conditions of the Acquisition. Forward-looking statements are necessarily based upon a number of estimates and assumptions that, while considered reasonable, are subject to known and unknown risks, uncertainties, and other factors which may cause the actual results and future events to differ materially from those expressed or implied by such forward-looking statements. Such factors include, but are not limited to: general business, economic, competitive, political and social uncertainties; and delay or failure to receive board, shareholder or regulatory approvals. There can be no assurance that such statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking statements. The Corporation disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

SOURCE: EastWest Bioscience Group

ReleaseID: 549718

Sanara MedTech Inc. Announces Expanded Line of Credit, Launch of BIAKOS(TM) Antimicrobial Skin & Wound Cleanser and Approval of Stock Purchase Program

FORT WORTH, TX / ACCESSWIRE / June 25, 2019 / Sanara MedTech Inc. (OTCQB: SMTI) Based in Fort Worth, Texas, Sanara MedTech Inc. (“Sanara” or the “Company”), a provider of surgical and chronic wound care products dedicated to improving patient outcomes, today announced (1) an expanded line of credit with Cadence Bank, (2) the launch of BIAKŌS™ Antimicrobial Skin & Wound Cleanser, and (3) the approval of a stock purchase program.

Expanded Line of Credit with Cadence Bank

The Company recently amended and expanded its line of credit with Cadence Bank from $1.0 million to $2.5 million. The expanded line of credit will provide the Company with additional working capital for its product pipeline, sales force expansion and other corporate purposes.

BIAKŌS™ Antimicrobial Skin & Wound Cleanser to Launch in July 2019

The Company announced that it expects to begin selling BIAKŌS™ Antimicrobial Skin & Wound Cleanser in July 2019 through its wound care distribution channels. BIAKŌS™ Antimicrobial Skin & Wound Cleanser is an FDA cleared patented wound cleansing spray that disrupts extracellular polymeric substances to eradicate biofilm. Various clinicians in selected post-acute care settings have experienced promising clinical results using BIAKŌS™ in conjunction with the Sanara HYCOL™ hydrolyzed collagen product.

Shawn Bowman, President, Wound Care Division, stated, “BIAKŌS™ Antimicrobial Skin & Wound Cleanser is a unique multi-functional solution which has demonstrated excellent clinical efficacy. This is a large opportunity and there is only one primary competitor in the marketplace. This competitor has a market cap of nearly $500 million and we believe our clinical results and existing distribution channels will allow us to quickly become the market leader in biofilm management.”

Approval of Stock Purchase Program

The Company’s Board of Directors has authorized the Company to purchase up to 5.0% of the current outstanding shares of the Company’s common stock from time to time in the open market or through privately negotiated transactions at prevailing market prices, depending on market conditions. The repurchase program has no time limit and may be discontinued at any time, however the Company will use its best efforts to complete the repurchase program by the end of 2019. All shares repurchased, whether through open market or privately negotiated transactions, will be restored to the status of authorized but unissued stock.

Ron Nixon, Executive Chairman of the Board, stated, “The Board fundamentally believes that the Company’s stock is undervalued at current prices and the stock repurchase program provides a meaningful way to deliver value to our shareholders.”

About Sanara MedTech Inc.

With our focus on improving patient outcomes with evidenced-based healing solutions, Sanara MedTech Inc. develops, markets and distributes biotechnology products to physicians, hospitals, clinics and all post-acute care settings. We continue to seek long-term strategic partnerships with a focus on products that complement our existing portfolio and provide more efficacious outcomes at a lower overall cost. Our products are sold in the North American advanced wound care and surgical tissue repair markets. Sanara MedTech Inc. sells and distributes CellerateRX® Surgical Activated Collagen® Adjuvant, HYCOL™ Hydrolyzed Collagen, BIAKŌS™ Antimicrobial Skin & Wound Cleanser and PULSAR II™ Advanced Wound Irrigation System (AWI™).

For more information, visit WNDM.com.

Information about Forward-Looking Statements

The statements in the press release that relate to the Company’s expectations with regard to the future impact on the Company’s results from new products in development and any other statements not constituting historical facts are “forward-looking statements,” within the meaning of and subject to the safe harbor created by the Private Securities Litigation Reform Act of 1995. Since this information may contain statements that involve risk and uncertainties and are subject to change at any time, the Company’s actual results may differ materially from expected results. This document may contain forward-looking statements concerning the Company’s operations, current and future performance and financial condition. These items involve risks, contingencies and uncertainties such as product demand, market and customer acceptance, the effect of economic conditions, competition, pricing, the ability to consummate and integrate acquisitions, and other risks, contingencies and uncertainties detailed in the Company’s SEC filings, which could cause the Company’s actual operating results, performance or business plans or prospects to differ materially from those expressed in, or implied by these statements. The Company undertakes no obligation to revise any of these statements to reflect the future circumstances or the occurrence of unanticipated events.

Investor Contacts:

Investor Relations
817-529-2300
ir@wndm.com

SOURCE: Sanara MedTech Inc.

ReleaseID: 549775

Experion Announces Letter of Intent with Polish Import and Distribution Company

VANCOUVER, BC / ACCESSWIRE / June 25, 2019 / Experion Holdings Ltd. (“Experion” or the “Company”) (TSXV: EXP) (OTCQB:EXPFF) (FRANKFURT:MB31), formerly Viridium Pacific Group Ltd., is pleased to announce that it has signed a non-binding Letter of Intent (”LOI”) with a Polish Import and distribution Company (”Polish Company”) to export medical flower products to Poland for scientific purposes.

The executed LOI consist of two parts, part one, will see Experion exporting medical flower products to Poland for scientific purposes enabling the Polish Company to test and develop Experion’s flower products. Upon the successful testing and development of the flower products and once a viable export and import channel has been established between Canada and Poland, part two of the LOI will commence which will see Experion exporting increased quantities of its flower products into Poland for medical use. Experion will also have completed its EU GMP certification which will allow for part two of the LOI.

Mr. Jay Garnett, Chief Executive Officer commented, “The LOI represents a major milestone for Experion. As medical marijuana becomes more legalized around the world, Experion continues to focus on the vast export market in countries with early opportunities. By exporting products for scientific research, we are able to move past barriers to entry and be one of the first Canadian producers to enter Poland”

Pursuant to the LOI, Experion and the Polish Import Company will work towards a definitive agreement as Experion seeks to increase export opportunities in Europe and continue to build Experion’s international distribution chain.

Mr. Jay Garnett further commented “I am truly proud of the work that the team has done and the great strides we have made to date. This is yet another result of solid teamwork that can only be achieved by having a shared vision and goal as we work diligently to unlock value for our most important asset and audience – our shareholders.

About Experion Holdings Ltd.

Experion Holdings Ltd. is the parent company of Experion Biotechnologies Inc., a Health Canada licensed cultivator and processor of Cannabis, based in Mission, BC; and EFX Laboratories Inc., a medical products production and clinical research company based in Calgary, AB.

Experion Holdings Ltd. is invested in a portfolio of products to address a wide spectrum of consumer needs’ including Medical, Adult-use, and Wellness and Therapeutic products.

For further information, please visit the Company’s website www.experionwellness.com or contact:

Experion Holdings Ltd

Judy-Ann Pottinger, Investor Relations
Tel: (604) 617-5290
judy-ann@experionwellness.com

We invite all investors and other interested parties to join the Experion Holdings portal on 8020 Connect. Join here: http://connects.company/Experion

Disclosure

This press release contains forward-looking information within the meaning of Canadian securities laws. Although the Company believes that such information is reasonable, it can give no assurance that such expectations will prove to be correct.

Forward looking information is typically identified by words such as: believe, expect, anticipate, intend, estimate, forecast, postulate and similar expressions, or are those, which, by their nature, refer to future events. The Company cautions investors that any forward-looking information provided by the Company are not guarantees of future results or performance, and that actual results may differ materially from those in forward looking information as a result of various factors, including, but not limited to: the state of the financial markets for the Company’s equity securities; recent market volatility; the Company’s ability to raise the necessary capital or to be fully able to implement its business strategies; the risks identified in the Filing Statement, and other risks and factors that the Company is unaware of at this time. The reader is referred to the Filing Statement dated September 25, 2017 and/or the most recent annual and interim Management’s Discussion and Analysis for a more complete discussion of such risk factors and their potential effects, copies of which may be accessed through the Company page on SEDAR at www.sedar.com.

SOURCE: Experion Holdings Ltd.

ReleaseID: 549774

Viveve Announces FDA 510(k) Clearance of Viveve 2.0 Next Generation System in the U.S.

Company also announces expansion of distribution network targeting gynecology practices in the Middle East through partnership with Dansys Group

ENGLEWOOD, CO / ACCESSWIRE / June 25, 2019 / Viveve Medical, Inc. (NASDAQ: VIVE), a medical technology company focused on women’s intimate health, today announced 510(k) K190422 clearance by the U.S. Food and Drug Administration (FDA) for the company’s next-generation Viveve 2.0 cryogen-cooled monopolar radiofrequency (CMRF) system for use in general surgical procedures for electrocoagulation and hemostasis.

“We are pleased to have received 510(k) clearance of the Viveve 2.0 System and its consumable treatment tips from the FDA, which is another important confirmation of the safety profile of our technology. This clearance is the most recent milestone in our ongoing regulatory strategy to expand the global commercial footprint of our next generation CMRF platform technology. In addition to bringing this innovative technology to patients in the U.S., this clearance can help streamline the regulatory pathway of our 2.0 technology in the Middle East and other important international markets,” said Scott Durbin, Viveve’s chief executive officer and director.

Distribution Partnership with Dansys Group

Viveve also announced establishment of a distribution agreement for the Viveve 2.0 System with Dansys Group LLC, a leading medical distributer in the Middle East. The agreement expands the distribution network for Viveve products throughout the Middle East.

“This new distribution partnership with Dansys Group will significantly expand our commercial footprint in the region through their large established customer base of gynecology practices, hospitals, and medical institutions. We look forward to working with an established and well-respected leader across the region in women’s health,” continued Mr. Durbin.

Mr. Jamil Maalouf, Dansys Group’s chief executive officer, commented, “It is a privilege to enhance our portfolio and offer our medical specialty practice and hospital customers the evidence-based treatments for women’s intimate health conditions that Viveve’s unique CMRF technology provides. Dansys Group is committed to women’s health innovation and recently hired Thomas B. McDermott as Vice President of Business Development. Thomas is a seasoned professional with a proven record of success in medical device sales and management, specifically with cutting-edge technology for women’s health procedures. He is excited to partner with Viveve and lead the expanded adoption and utilization of this innovative and proven-effective technology in the Gulf Region.”

About Viveve

Viveve Medical, Inc. is a medical technology company focused on women’s intimate health. Viveve is committed to advancing new solutions to improve women’s overall well-being and quality of life. The internationally patented Viveve® System incorporates cryogen-cooled monopolar radiofrequency (CMRF) technology to uniformly deliver volumetric heating while gently cooling surface tissue to generate neocollagenesis in a single in-office session.

International regulatory approvals and clearances have been received for vaginal laxity and/or improvement in sexual function indications in over 50 countries. Viveve is conducting VIVEVE II, a multicenter, randomized, double-blind, sham-controlled clinical trial to assess improvement of sexual function in women following vaginal childbirth. Completion of full 250 subject enrollment was announced in early March 2019. If successful, VIVEVE II results could support a marketing application for a new U.S. commercial indication. Currently, in the United States, the Viveve® System is cleared by the FDA for use in general surgical procedures for electrocoagulation and hemostasis.

Viveve has fully enrolled LIBERATE-International, one of two planned independent, multicenter, randomized registration trials for the improvement of stress urinary incontinence in women and plans to re-submit an IDE to the FDA for the LIBERATE-U.S. clinical trial after conducting certain safety testing. The results of these two trials, if successful, could support marketing applications in the U.S. and over 30 countries around the world for this new commercial indication.

For more information visit Viveve’s website at www.viveve.com.

Safe Harbor Statement

All statements in this press release that are not based on historical fact are “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. While management has based any forward-looking statements included in this press release on its current expectations, the information on which such expectations were based may change. These forward-looking statements rely on a number of assumptions concerning future events and are subject to a number of risks, uncertainties and other factors, many of which are outside of our control, which could cause actual results to materially differ from such statements. Such risks, uncertainties and other factors include, but are not limited to, the fluctuation of global economic conditions, the performance of management and our employees, our ability to obtain financing, our ability to obtain approval or clearance for sale of our medical device for all indications sought, competition, general economic conditions and other factors that are detailed in our periodic and current reports available for review at www.sec.gov. Furthermore, we operate in a highly competitive and rapidly changing environment where new and unanticipated risks may arise. Accordingly, investors should not place any reliance on forward-looking statements as a prediction of actual results. We disclaim any intention to, and undertake no obligation to, update or revise forward-looking statements to reflect events or circumstances that subsequently occur or of which we hereafter become aware, unless required by law.

Viveve is a registered trademark of Viveve, Inc.

Investor Relations contacts:

Sarah McCabe
Stern Investor Relations, Inc.
(212) 362-1200
sarah@sternir.com

Amato and Partners, LLC
Investor Relations Counsel
admin@amatoandpartners.com

Media contact:

Kelly Wakelee
Berry & Company Public Relations
(212) 253-8881
kwakelee@berrypr.com

SOURCE: Viveve Medical, Inc.

ReleaseID: 549772

Houston Hospital Pharmacy Equipment & Supplies Salvage Recovery Services Launch

Commercial Property Salvage of Houston, Texas announced that it can purchase damaged technology and hospital pharmacy equipment and supplies, helping clients in the medical industry and insurance adjusters minimize their losses and increase their ROI.

Houston, United States – June 25, 2019 /PressCable/

Commercial Property Salvage, a company based in Houston, Texas, launched an update of its services for clients in the medical industry, their representative attorneys and risk managers, as well as insurance adjusters. The company is a licensed medical recycler and can handle medical equipment and products in all 50 states, allowing clients to gain recovery for items which would otherwise have been considered as losses.

More information can be found at https://commercialpropertysalvage.com/adjusters-carriers-claims.

Damaged medical equipment and products can be difficult to sell, especially since many companies are not licensed to handle such items.

As a licensed pharmaceuticals handler and medical equipment recycler, Commercial Property Salvage aims to provide a complete turn key solutions for clients in the medical industry, as well as insurance adjusters.

The company buys a variety of damaged commercial property, including damaged equipment, medicine, automated medication dispensing cabinets, RX medication carts, RX-robots (pharmacy dispensing robots), medical therapeutic products, electronics and inventory.

They are licensed to handle all hospital pharmacy equipment and emergency life saving stock & supplies.

Commercial Property Salvage can handle all types of damaged goods, including fire and water damage, contamination, and more. Working with the Houston salvage experts, adjusters will be able to lower their loss-ratio limit and increase their recovery value.

With the recent update, the Houston company continues to expand its range of services for commercial, legal and insurance clients in Houston and nationwide.

Commercial Property Salvage specializes in medical, technology and offset sheet presses, but can also work with other types of damaged items. The company focuses on reusable equipment and medium to large salvage losses.

A spokesperson for the company explained: “Salvage is more than just scrap, in the commercial property industry it very often still holds considerable value. We focus on the sales of high technology electronics, medical equipment & lithographic presses which holds good salvage value. The property salvage we focus on usually is not going to be just a part’s machine nor scrap. Equipment focus is on reusable and rebuildable or repairable assets.”

Interested parties can find more information by visiting the above-mentioned website, as well as at https://www.youtube.com/watch?v=k9Ynup9ls7M.

Contact Info:
Name: Robert Alexander
Email: Send Email
Organization: Robert Alexander
Address: Houston, Texas, Houston, Texas, United States
Phone: +1-281-905-1574
Website: https://commercialpropertysalvage.com

Source: PressCable

Release ID: 527997

Color Caricature Drawing From Photo Online Cartoon Portrait Services Announced

Nick Polydoros announcers his caricature drawing services in Houston Texas. He is an artist with over four decades of experience. He creates both black and white and color drawings live and from photographs. Nick also creates group drawings.

Houston, United States – June 25, 2019 /PressCable/

Nick Polydoros announces color and black and white caricature drawings for individuals, events, and parties. The drawing can be made from a photograph or done live.

For more information visit their website at https://caricatures-by-nick-polydoros.business.site

People want special events to be remembered. Whether it is a party, a milestone event or the grand opening of a new shop or establishment, the event is best commemorated through photograph and video and now through a drawing of the different scenarios as they unfold.

Nick Polydoros has been working as a professional caricature artist for over 44 years. He is recognized as among the best in Houston Texas by his peers. He does both pencil drawings and black and white vintage style caricature drawings. A specialty of Nick Polydoros is his watercolor coloring by hand of his caricature drawings.

At any fundraiser or company event, a live caricaturist at the venue is a sure way to add excitement and a touch of fun. Unique moments at trade shows, corporate promotion events, awards, and special days such as birthdays or Bar Mitzvah celebrations, can be captured dynamically if an artist is present at the venue.

All Nick Polydoros’ drawings are customized to the people who are his subjects. Nick offers his services also to small events such as weddings, private parties, picnics, and even small group dinners. He also draws group caricatures in black and white or color.

A specialty is drawing freehand color caricatures from print or digital photographs. He also is able to fill in drawings with colored ink. For those who like to transform a color photograph into an old world black and white drawing, Nick is able to provide perfect solutions.

The final price will be e determined by factors such as the size and complexity of the photograph, the number of people in the photograph, the level of customization and the primary and secondary sizes of the people. Nick is known to be very competitively priced and affordable in the industry.

For more information visit their website given above or call them on +1-713-261-6373.

Contact Info:
Name: Nick Polydors
Email: Send Email
Organization: Caricatures By Nick Polydoros
Address: Houston Texas, Houston, TX, United States
Phone: +1-713-261-6373
Website: https://caricatures-by-nick-polydoros.business.site

Source: PressCable

Release ID: 88889175

Insurance Experts Present Several Ways To Get Cheaper Car Insurance Rates

LOS ANGELES, CA / ACCESSWIRE / June 25, 2019 / Compare-autoinsurance.org has released a new blog post that informs policyholders how to make the auto insurance premiums cheaper.

For more info and free car insurance quotes online, visit https://compare-autoinsurance.org/lower-car-insurance-premiums/

Car insurance premiums are determined after analyzing a multitude of factors. Some of them are under direct policyholder’s control, thus helping him to keep prices under control or even lower the costs.

In order to get better prices, it is recommended to:

Set higher deductibles. Deductibles are paid by the client after filing a claim. After the client pays his share, the insurer will pay the difference. By selecting a higher deductible, the client will assume more financial responsibility and he will be rewarded with cheaper premiums. Many insurance companies allow the driver to select the deductible and the quote will be adjusted.

Install anti-theft devices. Lowering the risk of having the car stolen will be greatly rewarded by insurance companies. Comprehensive car insurance is the policy which covers car theft. And it is really pricey. By adding anti-theft and tracking devices, premiums will be significantly lowered by the insurer. Look for the best devices on the market and read some reviews. Again, when getting online quotes, the user is asked about alarms and anti-theft devices.

Install safety and recovery devices. No matter if the car is a top safety pick or just an average model, adding extra safety devices is money-worth. However, it is important to notify the current insurer before actually installing aftermarket devices. Ask if the added components qualify the car for a safety gear discount. Many online questionnaires ask about installed safety features.

Park the car in a safe location. During online quotes, the driver may be asked to provide the address or ZIP code for the place where the car is usually parked. The place where the car is parked is a top influential factor. It is strictly linked with car theft incidence, riots and vandalism. The best place to park the car overnight is inside a locked garage.
Bundle multiple insurance policies. Bundling insurance policies is a smart way to get cheaper premiums. Usually, it is cheaper to combine multiple insurance services or multiple vehicles under the same contract. However, a policyholder should compare prices after and before bundling and check if he will really save money. There is also a limit to the number of insured cars. Families with more than one car should apply for multi-vehicle plans.

Pay the entire coverage in advances Choosing to pay for the whole coverage in advance will help the company avoid monthly installment fees. The policyholder will receive cheaper premiums since those costs are no longer added.

Driving less than a certain limit will drastically reduce insurance costs. Spending less time on the roads means that the driver is less exposed to accidents and filing claims. Check what “low mileage” means for the insurance company.

Consider insurance costs before purchasing a car. It is recommended to get online car insurance quotes before buying a car. Insurance must not be an afterthought. Also, keep in mind that rates vary widely among insurance providers.

“Besides using online quotes, there are other ways to get cheaper car insurance. Check our website to find out more tips and strategies for lowering the premiums.” said Russell Rabichev, Marketing Director of Internet Marketing Company.

Compare-autoinsurance.org is an online provider of life, home, health, and auto insurance quotes. This website is unique because it does not simply stick to one kind of insurance provider, but brings the clients the best deals from many different online insurance carriers. In this way, clients have access to offers from multiple carriers all in one place: this website. On this site, customers have access to quotes for insurance plans from various agencies, such as local or nationwide agencies, brand names insurance companies, etc.

For more information, please visit http://compare-autoinsurance.org

Contact: cgurgu@internetmarketingcompany.biz

SOURCE: Internet Marketing Company

ReleaseID: 549786

Aytu BioScience Announces First Clinical Results Demonstrating Clinical Utility of MiOXSYS Male Infertility Test When Used Prior to In Vitro Fertilization (IVF) Procedures

First Clinical Data Demonstrating Predictive Power of Seminal Oxidation-Reduction Potential (ORP) as a Predictor of Fertilization When Used Prior to IVF

ENGLEWOOD, CO / ACCESSWIRE / June 25, 2019 / Aytu BioScience, Inc. (NASDAQ: AYTU), a specialty pharmaceutical company focused on commercializing novel products that address significant patient needs, announced the presentation of novel clinical data demonstrating the predictive power of the company’s MiOXSYS® male infertility diagnostic system in assessing fertilization outcomes following In Vitro Fertilization (IVF).

These clinical studies are the first to demonstrate the predictive power of oxidation-reduction potential (ORP), the diagnostic output of the MiOXSYS System, in determining fertilization outcomes following artificial insemination procedures. When measured in semen samples prior to the introduction of sperm via both IVF and Intracytoplasmic Sperm Injection (ISCI) procedures, both studies reported that oxidation-reduction potential was highly predictive of fertilization.

Two MiOXSYS clinical studies were presented on June 24, 2019 at the 35th Annual Meeting of the European Society of Human Reproduction and Embryology (ESHRE) in Vienna, Austria.

The studies are detailed below.

Study #1

“Prediction of Successful ICSI Cycles by Oxidation-Reduction Potential (ORP) and Sperm DNA Fragmentation (SDF) Analysis”

Principal Investigator:

Ralf Henkel, PhD, Professor
Department of Medical Biosciences
University of Western Cape, Bellville, South Africa

Study Summary:

The study utilized 51 ejaculated semen samples and conducted sperm preparation for ICSI and oxidative stress measurement via ORP measurement with the MiOXSYS System. Sperm DNA fragmentation analysis was conducted via TUNEL assay.

Key Result:

When using an ORP cutoff value of 1.36 mV/106 sperm/mL, the predictive power of ORP for fertilization was 81.3% following ICSI (p=.0002).

Conclusions:

This study demonstrated strong predictive capabilities of ORP (oxidation-reduction potential, as measured by the MiOXSYS System) measurement in the clinical setting.
ORP is clinically useful in providing the clinician with a valuable diagnostic tool for prediction of fertilization in ICSI cycles.
When used in conjunction with semen analysis, ORP can be used to predict and improve the likelihood of fertilization outcomes.

Dr. Ralf Henkel, the study’s principal investigator and Professor at the University of Western Cape, commented, “Having done functional andrological diagnostics for more than 20 years, I have seen the progress andrological diagnostics have made. Now, for the first time, an easy, standardized and therefore properly quantifiable parameter is available, which correlates very well with semen quality and fertilization after assisted reproductive techniques. This is a major step forward in the right direction.”

Study #2

“Relationship Between Oxidative Stress in Semen and the Fertilizing Capacity of the Sperm – Evidence from the Conventional IVF Model in Couples with Unexplained Infertility”

Principal Investigator:

Hassan Sallam MD, PhD, Professor of Obstetrics and Gynecology
Head, Alexandria Fertility and IVF Center
University of Alexandria, Alexandria, Egypt

Study Summary:

This prospective study was conducted between September 2017 and December 2018, and 25 couples with unexplained infertility were included in the cohort. Couples were treated for one cycle of combined IVF/ICSI if 12 oocytes or more were retrieved. Oxidation-reduction potential (ORP) was determined in native semen samples by measuring ORP using the MiOXSYS System to assess correlation of ORP with fertilization rates.

Key Results:

Seminal ORP as measured by the MiOXSYS System, using a cutoff value of 1.5692 mV/106 sperm/mL, demonstrated a positive likelihood ratio (+LR) of 80.0% among IVF/ICSI couples who had greater than or equal to 50% fertilization of oocytes.
The mean ORP in the native semen in couples with =>50% IVF fertilization was 1.02 ± 0.1 mV/106 sperm/mL which is significantly lower than in couples with <50% fertilization (2.05 ± 0.7 mV/106 sperm/mL) (P<0.02).
Seminal ORP as measured by the MiOXSYS System, effectively distinguished between those couples above and below 50% fertilization rates.

Conclusion:

Measuring ORP in native semen can/should be used in couples with unexplained or male factor infertility to help determine the best management option: antioxidant therapy, intrauterine insemination (IUI), in-vitro fertilization (IVF), and intra-cytoplasmic sperm injection (ICSI).

Dr. Hassan Sallam, MD, PhD, the study’s principal investigator and Professor of Obstetrics & Gynecology at Alexandria University, concluded, “This study offers conclusive evidence that ORP (as measured via the MiOXSYS System) is negatively and significantly related to the fertilizing capacity of the spermatozoa.”

The MiOXSYS System is currently in use in over thirty countries around the world, and is CE Marked and cleared by Health Canada, the Australian Therapeutic Goods Administration (TGA), and Mexico’s COFEPRAS.

Selection of the abstracts for publication or presentation in this press release does not imply endorsement of the MiOXSYS System by ESHRE.

About Aytu BioScience, Inc.

Aytu BioScience is a commercial-stage specialty pharmaceutical company focused on commercializing novel products that address significant patient needs. The company currently markets Natesto®, the only FDA-approved nasal formulation of testosterone for men with hypogonadism (low testosterone, or “Low T”). Aytu also has exclusive U.S. and Canadian rights to ZolpiMist™, an FDA-approved, commercial-stage prescription sleep aid indicated for the short-term treatment of insomnia characterized by difficulties with sleep initiation. Aytu recently acquired exclusive U.S. commercial rights to Tuzistra® XR, the only FDA-approved 12-hour codeine-based antitussive syrup. Tuzistra XR is a prescription antitussive consisting of codeine polistirex and chlorpheniramine polistirex in an extended-release oral suspension. Additionally, Aytu is developing MiOXSYS®, a novel, rapid semen analysis system with the potential to become a standard of care for the diagnosis and management of male infertility caused by oxidative stress. MiOXSYS is commercialized outside of the U.S. where it is a CE Marked, Health Canada cleared, Australian TGA approved, Mexican COFEPRAS approved product, and Aytu is planning U.S.-based clinical trials in pursuit of 510k de novo medical device clearance by the FDA. Aytu’s strategy is to continue building its portfolio of revenue-generating products, leveraging its focused commercial team and expertise to build leading brands within large therapeutic markets. For more information visit aytubio.com.

Forward-Looking Statements

This press release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, or the Exchange Act. All statements other than statements of historical facts contained in this presentation are forward-looking statements. Forward-looking statements are generally written in the future tense and/or are preceded by words such as ”may,” ”will,” ”should,” ”forecast,” ”could,” ”expect,” ”suggest,” ”believe,” ”estimate,” ”continue,” ”anticipate,” ”intend,” ”plan,” or similar words, or the negatives of such terms or other variations on such terms or comparable terminology. These statements are just predictions and are subject to risks and uncertainties that could cause the actual events or results to differ materially. These risks and uncertainties include, among others: risks relating to gaining market acceptance of our products, obtaining reimbursement by third-party payors, the potential future commercialization of our product candidates, the anticipated start dates, durations and completion dates, as well as the potential future results, of our ongoing and future clinical trials, the anticipated designs of our future clinical trials, anticipated future regulatory submissions and events, our anticipated future revenue growth, our anticipated future cash position and future events under our current and potential future collaboration. We also refer you to the risks described in ”Risk Factors” in Part I, Item 1A of Aytu BioScience, Inc.’s Annual Report on Form 10-K and in the other reports and documents we file with the Securities and Exchange Commission from time to time.

Contact for Investors:

James Carbonara
Hayden IR
(646)-755-7412

SOURCE: Aytu BioScience, Inc.

ReleaseID: 549410

Envision Solar Adds First Major Pharmaceutical Company to Growing Roster of Customers

Deployment Marks Envision’s First in Massachusetts

SAN DIEGO, CA / ACCESSWIRE / June 25, 2019 / Envision Solar International, Inc., (Nasdaq CM: EVSI, EVSIW) (“Envision Solar,” or the “Company”), the leading producer of unique and sustainable infrastructure products for electric vehicle charging, energy security and outdoor media, today announced that it has received the first order for its EV ARC™ product from a major Massachusetts-based pharmaceutical company.

The new customer chose Envision’s solar-powered and rapidly deployable EV ARC™ product because of its ease of installation and because it provides a highly visible demonstration of its commitment to the environment, while encouraging its employees to reduce their carbon footprint through commuting in electric vehicles powered by the sun. The EV ARC™ will deliver true zero-emissions EV charging for the company’s employees, without environmental impact, the need for permitting, construction or a utility connection or resultant bill. The ability to add distributed, transportable, solar powered chargers, as EVs become more widely adopted, without planning, construction or grid upgrades, makes the EV ARC™ product the ideal solution for the company’s growing EV charging demand. Free solar-powered EV charging is a compelling employee benefit offered by the pharmaceutical company.

“This pharmaceutical company has demonstrated a commitment to reducing its carbon footprint and represents a new industry to recognize the benefits of driving on sunshine with our EV ARCs,” said Desmond Wheatley, CEO of Envision Solar. “We are delighted to support their expanding efforts to benefit from our clean, green, impact-free charging infrastructure. We believe more and more companies across a growing array of industries will recognize, as our new customer has, that Envision’s zero impact, rapidly deployable EV charging infrastructure is not just a truly economical, environmentally conscious EV charging energy alternative, it is the future of fuel.”

Invented and manufactured in California, the patented EV ARC™ and EV ARC™ HP products fit inside single parking spaces without reducing available parking. EV ARC™ generates enough clean solar electricity to power up to 225 miles of EV driving in a day. EV ARC™ HP DC fast charging systems provide up to 1,100 miles per day. The EV ARC™ system’s solar electrical generation is enhanced by EnvisionTrak™ (patented) which causes the solar array to follow the sun, generating up to 25 percent more electricity than a fixed array. The energy is stored in the EV ARC™ product’s on-board energy storage for charging day or night, and provides EV charging and emergency power during grid failure. The EV ARC™ product is a permanent solution that provides Level I, Level II and DC Fast Charging but because it requires no trenching, foundations or installation work of any kind, is deployed in minutes and can be moved to a new location with ease. EV ARC™ products are manufactured in the company’s San Diego facility by highly talented, mission-driven team members, including combat veterans, individuals with disabilities and other underserved demographics.

About Envision Solar International, Inc.

Envision Solar, www.envisionsolar.com, is a sustainable technology innovation company whose unique and patented products include the EV ARC™ and the Solar Tree® with EnvisionTrak™ patented solar tracking, SunCharge™ solar Electric Vehicle Charging, ARC™ technology energy storage, and EnvisionMedia solar advertising displays.

Based in San Diego, the company produces Made in America products. Envision Solar is listed on the NasdaqCM under the symbols EVSI and EVSIW. For more information visit www.envisionsolar.com or call (858) 799-4583. Follow us on social media to keep up with the latest news: Facebook, Twitter, Instagram, and YouTube.

Forward-Looking Statements

This Envision Solar International, Inc., press release may contain forward-looking statements, including those related to the closing of the offering. All statements in this Press Release other than statements of historical facts are forward-looking statements. Forward-looking statements are generally accompanied by terms or phrases such as “estimate,” “project,” “predict,” “believe,” “expect,” “anticipate,” “target,” “plan,” “intend,” “seek,” “goal,” “will,” “should,” “may,” or other words and similar expressions that convey the uncertainty of future events or results.

Media Contact:

Lucia Asbury
Envision Solar International, Inc.
(858) 799-4583
gosolar@envisionsolar.com

Investor Relations:

Tristan Traywick
Senior Account Director
CORE IR
516 222 2560
tt@coreir.com
www.coreir.com

SOURCE: Envision Solar International, Inc.

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