HOUSTON, TX (Marketwiredon September 21, 2017) – AngioSoma, Inc. (OTC: SOAN) — Esther & Esther management has high optimism that its revenue plan could prove successful. The publicly stated plan simply and efficiently drives high volume traffic and interested buyers directly to EstherandEsther.com.
As noted in the previous press release (which can be read here), SOAN is capitalizing the Joint Venture of the successful EstherandEsther.com. The JV intends to increase its revenue by: 1) Implementing a simple and powerful sales and marketing action plan; 2) Developing a new website optimized for accelerated growth, and; 3) Scaling and automating administrative function to efficiently manage and report the anticipated growth.
The corporate strategy to achieve sales goals is to effectively market Soma Nutraceutical and E&E products directly through highly influential social media influencers. The company has established sufficient capital to hire and manage up to 100 Promotional Model Independent Contractors with significant media influence to promote, vet and attract potential customers to EstherandEsther.com. Esther and Esther has had significant success in its current market sectors and is seasoned to expand its retail presence in large markets throughout the U.S., utilizing its online Etail store as the operational platform. Extending retail sales and distribution of carried and inhouse brands in the low cost / High Yield, sales model offered by the platform approach, favorably increases both the JV’s odds of success and the speed at which higher, potentially much higher, revenue forecasts may be achieved.
To learn more about the JV’s plans to hire and manage its long term Promotional Model Independent Contractors go to: https://www.facebook.com/estherandesther/
ABOUT ANGIOSOMA, INC.
AngioSoma, Inc. (http://www.angiosoma.com) is a clinical stage biopharmaceutical company focused on improving the effectiveness of current standard-of-care treatments, especially related to endovascular interventions in the treatment of peripheral artery disease (‘PAD‘). Our lead pharmaceutical product Liprostin™, a treatment for PAD, has successfully completed FDA Phase I and three Phase II clinical trials, and we are in discussions with several contract research organizations for rapid completion of our U.S. Food and Drug Administration (‘FDA‘) approved protocol for Phase III with submission of our new drug application for marketing in the U.S. and its territories.
NOTICE REGARDING FORWARD LOOKING STATEMENTS
This news release contains forward-looking information within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, including statements that include the words “believes,” “expects,” “anticipate” or similar expressions. Such forward-looking statements involve known and unknown risks, and other factors that may cause the actual results, performance or achievements of the company to differ materially from those expressed or implied by such forward-looking statements. In addition, description of anyone’s past success is no guarantee of future success. This news release speaks as of the date first set forth above and the company assumes no responsibility to update the information included herein for events occurring after the date hereof.