To: Ron Sigourney who wrote (780 ) 11/18/1997 6:50:00 PM From: Scott Kelly Respond to of 7041
Harvard Scientific's Board of Directors Appoints Thomas E. Waite asIts New President, CEO and Chairman of the BoardRENO, Nevada, Nov. 18 /PRNewswire/ -- Harvard Scientific Corp. (OTCBulletin Board: HVSF), a Nevada corporation, announced today thatits Board of Directors has appointed Thomas E. Waite as presidentand CEO of the company. Mr. Waite will also serve as Chairman ofthe Board of Directors. Mr. Waite brings to the company years ofdirect experience in the company's business operations andpreviously served the company as a consultant. Prior to his appointment, Waite was the President of Thomas E.Waite & Associates in Lake Mary, FL, a consulting firm thatspecialized in the areas of investment banking, corporate finance,merger/acquisitions and public relations for publicly tradedcompanies. As part of Waite's employment agreement, he has agreedto divest his current interests in Thomas E, Waite & Associates andto concentrate his effort full time to the affairs of the company. In an interview, Waite stated, "My first concern and priority isto strengthen the company's balance sheet while at the same timedesigning a concise road map which the company can follow throughthe Phase II/III clinical trials and the marketing of its products. I believe the issuance of the company's patent for its ProstaglandinE-1 (PGE-1) erectile dysfunction product has greatly enhanced itsability to compete in the U.S. market as well as strengthening itsposition worldwide." Harvard Scientific Corp. is a biopharmaceutical company thatdevelops, markets and distributes products relating to liposomaldelivery of PGE-1 for the treatment of male erectile dysfunction,impotency and sexual enhancement. The company's patent pendingprocess allows the PGE-1 to be administered as a liquid via apainless delivery system, PGE-1 is a naturally occurring vasodilatororiginally approved by the U.S. FDA for intravenous infusion inneonates. PGE-1 was first approved by the FDA for Upjohn'streatment for male erectile dysfunction via needle injection in 1995and approved in November, 1996, for Vivus, Inc.'s MUSE deliverysystems. The company believes its product represents a tremendoustreatment advantage over other delivery systems currently beingutilized in the industry. From time to time the company may issue forward-lookingstatements which involve risks and uncertainties. This news releasemay contain forward- looking statements within the meaning ofSection 27A of the Securities Act of 1933, as amended, and Section21E of the Securities Exchange Act of 1934, as amended. Actualresults could differ and any forward-looking statements should beconsidered accordingly,SOURCE Harvard Scientific Corp. 11/18/97/CONTACT: Irwin Miller of I.W. Miller & Co., Inc., 800-691-9991/ /Web site: harvardscientific.com (HVSF)