Mediware Delivers Key Support for Emerging U.S. Biovigilance Network
LENEXA, KS--(Marketwire - December 22, 2009) - Continuing its diligent focus on patient safety, [ Mediware Information Systems, Inc ]. (
Development of the U.S. Biovigilance Network was initiated to provide core metrics for transfusion reactions and the use of biologics in patient care. The network's goal is to collect comprehensive information from all suppliers and users of these biologic materials and enable detailed analysis that will ultimately help reduce adverse events associated with blood transfusion and related biological therapies.
"Electronic interfaces will enhance data accuracy and increase blood center participation in the national donor hemovigilance system," said Barbee I. Whitaker, PhD, who is director of data and special programs for AABB (formerly the American Association of Blood Banks) and one of the primary partners in the development of the U.S. Biovigilance Network. "Blood center response to live demonstrations at AABB's 2009 Annual Meeting and TXPO in New Orleans was very enthusiastic, and we look forward to the system release in March 2010."
"We were pleased to be in a position to leverage our open technology to quickly deliver an interface that will help increase participation in this important industry campaign," said Noel Strong, Mediware's vice president of research and development and chief technology officer.
Four components will eventually make up the U.S. Biovigilance Network: 1) the donor hemovigilance module, which will track adverse reactions associated with the donation process; 2) the hemovigilance module of the Centers for Disease Control and Prevention's National Healthcare Safety Network, which will track adverse events associated with transfusion of blood and blood components; 3) a tissue and organ adverse event reporting system; and 4) a cell therapy module.
Mediware's interface occurs between the donor hemovigilance module and the company's LifeTrak software; however, Mediware is actively working with subcommittees to design additional interfaces as specifications for the other modules are developed. Mediware expects to support the hemovigilance module of the NHSN with an interface to the Company's market leading HCLL™ Transfusion software. Tissue and cell therapy data will be provided through an interface to the Company's biologics management product, BiologiCare™.
"LifeTrak is used by some of the largest blood centers in the country and, by our estimates, collects most of the data desired by the Network," continued Mr. Strong. "Rather than having to re-key this information into the network's systems, our customers will be able to point and click to participate in this important initiative without any additional labor or impact on their business."
The LifeTrak system has a prestigious customer base and impressive market momentum, with Mediware announcing seven new customers in the past year. Some of these include the BloodCenter of Wisconsin, Carter Bloodcare, Central Jersey Blood Center, Blood Bank of Alaska, Heartland Community Blood Center, and Naples Community Blood Center. Several large hospital blood banks and centralized testing facilities also utilize LifeTrak to ensure safe and efficient blood donor management and blood manufacturing processes.
About Mediware
Mediware delivers interoperable best-of-breed software systems that integrate with electronic medical records to improve efficiencies and address safety concerns to enable healthcare organizations to improve care processes while decreasing costs. Core Mediware solutions include blood management technologies for hospitals and blood centers; medication management solutions for hospitals, behavioral health facilities, infusion and specialty pharmacy providers; and business intelligence-based performance management solutions for clinical, regulatory and financial aspects of the broader healthcare market. For more information about Mediware products and services, visit our web site at [ www.mediware.com ].
Certain statements in this press release may constitute "forward-looking" statements within the meaning of the Private Securities Litigation Reform Act of 1995, as the same may be amended from time to time (the "Act") and in releases made by the SEC from time to time. Such forward-looking statements are not based on historical facts and involve known and unknown risks, uncertainties and other factors disclosed in the Company's Annual Report on Form 10-K for the year ended June 30, 2009, which may cause the actual results of the Company to be materially different from any future results expressed or implied by such forward-looking statements. The Company disclaims any obligation to update its forward-looking statements.