Respected Plastic and Reconstructive Surgeon, Richard Simman, MD, Joins RenovaCare, Inc.

Dr. Richard Simman, Advisor, RenovaCare, Inc. (Photo: Business Wire)

NEW YORK & PITTSBURGH--()--RenovaCare, Inc., developer of the patented CellMist™ and SkinGun™ technologies* for isolating and spraying a patient’s own stem cells onto burns and wounds for rapid self-healing, today announced the appointment of board certified plastic and reconstructive surgeon, Richard Simman, MD, FACS, and FACCWS, to its Board of Advisors.

Dr. Simman is founding President and Chair of the American Board of Wound Medicine and Surgery, and past President of the American College of Clinical Wound specialists (ACCWS). He is current Editor-in-Chief of the Journal of the ACCWS, Professor of Pharmacology and Toxicology, and Associate Clinical Professor of Plastic and Reconstructive Surgery and Dermatology at Wright State University Boonshoft School of Medicine.

“What’s so unique about the RenovaCare CellMist™ system is by applying just one application using the SkinGun™ we render the second degree burn patient an incredible service – we’ve taken away his pain and accelerated his healing process,” said Dr. Simman. “I think that makes this technology very unique in the capability of immediate preparation and application.”

“Dr. Simman brings exceptional wound care expertise to the company as a highly sought-after and active clinician and researcher,” said Thomas Bold, President and CEO of RenovaCare, Inc. “It is a pleasure to welcome Dr. Simman to the team and I look forward to working with him to facilitate growth for our future commercial products, while advancing the clinical pipeline.”

Dr. Simman’s work has been published in numerous major journals including, Plastic and Reconstructive Surgery, Annals of Plastic Surgery, Aesthetics of Plastic Surgery, The Journal of Craniofacial Surgery, Wounds, Academic Emergency Medicine, and others. He is an active member of numerous medical associations.

Dr. Simman trained in General Surgery at St. Luke’s-Roosevelt Hospital Center, Columbia University in New York, NY and completed his Plastic Surgery residency at Providence Hospital and Medical Centers in Southfield, MI under the supervision of Dr. Ian T. Jackson, a world famous plastic surgeon. In addition, he completed a Burn Fellowship followed by a wound healing and cultured keratinocytes Research Fellowship at the State University of New York at Stony Brook. He has published over 80 peer-reviewed papers, abstracts and book chapters.

*RenovaCare products are currently in development. They are not available for sale in the United States.

About RenovaCare

RenovaCare, Inc. is developing first-of-their-kind autologous (self-donated) stem cell therapies for the regeneration of human organs. Its initial product under development targets the body’s largest organ, the skin. The company’s flagship technology, the CellMist™ System, uses its patented SkinGun™ to spray a liquid suspension of a patient’s stem cells – the CellMist™ Solution – onto wounds. RenovaCare is developing its CellMist™ System as a promising new alternative for patients suffering from burns, chronic and acute wounds, and scars. In the US alone, this $45 billion market is greater than the spending on high-blood pressure management, cholesterol treatments, and back pain therapeutics.

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No statement herein should be considered an offer or a solicitation of an offer for the purchase or sale of any securities. This release contains forward-looking statements that are based upon current expectations or beliefs, as well as a number of assumptions about future events. Although RenovaCare, Inc. (the “Company”) believes that the expectations reflected in the forward-looking statements and the assumptions upon which they are based are reasonable, it can give no assurance that such expectations and assumptions will prove to have been correct. Forward-looking statements, which involve assumptions and describe our future plans, strategies, and expectations, are generally identifiable by use of the words “may,” “will,” “should,” “could,” “expect,” “anticipate,” “estimate,” “believe,” “intend,” or “project” or the negative of these words or other variations on these words or comparable terminology. The reader is cautioned not to put undue reliance on these forward-looking statements, as these statements are subject to numerous factors and uncertainties, including but not limited to: the timing and success of clinical and preclinical studies of product candidates, the potential timing and success of the Company’s product programs through their individual product development and regulatory approval processes, adverse economic conditions, intense competition, lack of meaningful research results, entry of new competitors and products, inadequate capital, unexpected costs and operating deficits, increases in general and administrative costs, termination of contracts or agreements, obsolescence of the Company's technologies, technical problems with the Company's research, price increases for supplies and components, litigation and administrative proceedings involving the Company, the possible acquisition of new businesses or technologies that result in operating losses or that do not perform as anticipated, unanticipated losses, the possible fluctuation and volatility of the Company's operating results, financial condition and stock price, losses incurred in litigating and settling cases, dilution in the Company's ownership of its business, adverse publicity and news coverage, inability to carry out research, development and commercialization plans, loss or retirement of key executives and research scientists, and other risks. There can be no assurance that further research and development will validate and support the results of our preliminary research and studies. Further, there can be no assurance that the necessary regulatory approvals will be obtained or that the Company will be able to develop commercially viable products on the basis of its technologies. In addition, other factors that could cause actual results to differ materially are discussed in the Company's most recent Form 10-Q and Form 10-K filings with the Securities and Exchange Commission. These reports and filings may be inspected and copied at the Public Reference Room maintained by the U.S. Securities & Exchange Commission at 100 F Street, N.E., Washington, D.C. 20549. You can obtain information about operation of the Public Reference Room by calling the U.S. Securities & Exchange Commission at 1-800-SEC-0330. The U.S. Securities & Exchange Commission also maintains an Internet site that contains reports, proxy and information statements, and other information regarding issuers that file electronically with the U.S. Securities & Exchange Commission at http://www.sec.gov. The Company undertakes no obligation to publicly release the results of any revisions to these forward-looking statements that may be made to reflect the events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

Contacts

Media:
TrendLogic
Dwain Schenck, 800-992-6299
dwain@trendlogicpr.com

Contacts

Media:
TrendLogic
Dwain Schenck, 800-992-6299
dwain@trendlogicpr.com