Medifirst Solutions Inc. updated shareholders regarding recent company developments. As previously announced, Medifirst Solutions Inc., received 510(k) clearance from the U.S. Food and Drug Administration to market its infrared Time Machine TTML-8102000 Laser Thermal Therapeutic Device. Medifirst announced that it has made substantial progress in setting up its infrastructure for sales and compliance. The Company has engaged MDI Consultants, a provider of quality assurance, regulatory compliance, FDA consulting and clinical services to the healthcare industry. MDI Consultants will be hands-on with assisting and overseeing the implementation of the Company's internal controls and procedures as mandated by the FDA. These controls and procedures will be implemented in the Company's sales office, as well as at its manufacturer's facility.