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XStream Systems Chooses Medication Safety Expert for New VP of Business Development
Pat Earl, a pharmaceutical industry veteran with medication safety expertise in hospital and wholesale distribution settings, has joined XStream Systems as Vice President of Business Development.
Mrs. Earl has been actively involved in the pharmaceutical wholesale distribution industry since joining Meyers and Company, a predecessor of AmerisourceBergen Drug Company, in 1986. She has held a variety of management positions at AmerisourceBergen including Vice President General Manager of their Toledo, Ohio Division and Corporate Vice President of Strategic Development for Health Systems and Alternate Care. Pat developed and implemented the hospital and alternate care segment’s strategic initiatives. She played a significant role in the strategic positioning of the drug company’s technology and service offerings that enhanced patient safety at dispensing and bedside, as well as, increased operational efficiencies that provided cost savings to the health systems and alternate care providers.
Most recently, Pat was the Vice President of Drug Divisions and Vice President of Institutional Marketing at H. D. Smith. She has served on a number of HDMA and industry groups that focused on improving medication safety at the wholesale distribution level through eliminating unsafe practices in the supply chain.
XStream Systems, Inc. has a unique and innovative solution to eliminate the record number of counterfeit and adulterated pharmaceutical products entering the worldwide marketplace. The trend of counterfeit pharmaceuticals is problematic and represents a major National Security risk in the United States. The Prescription Drug Marketing Act of 1987 (PDMA) was enacted (1) to ensure that drugs purchased by consumers are safe and effective, and (2) to avoid the unacceptable risk to American consumers from counterfeit, adulterated, misbranded, sub-potent or expired drugs. The legislation was necessary to increase safeguards in the drug distribution process and to prevent the introduction and retail sale of substandard, ineffective or counterfeit drugs. Recently XStream Systems, Inc. has seen that the Federal and State regulatory agencies have established various Pedigree requirements in an attempt to address these critical issues. However, the Pedigree requirements do not include authentication and validation of the actual drugs. It is believed that the number of counterfeit and contaminated drugs will continue to increase unless effective countermeasures can be deployed. The most definitive way to effectively protect U.S. consumers is by verifying a drug’s efficacy at each ‘transfer point’ along the U.S. Supply Chain.
“Pat’s role as Vice President Business Development at XStream will be focused on implementing Pharmaceutical Supply Chain strategies to increase market penetration of the XT250TM Materials Identification Systems with pharmaceutical distributors, drug wholesalers, manufacturers and reverse distributors. Her experience and past success in pharmaceutical distribution industry is a perfect fit for XStream, “ stated Alan Clock, Senior Vice President at XStream Systems.
XStream Systems, Inc. offers unique patented systems based on Energy-Dispersive X-Ray Diffraction (EDXRD), a highly sophisticated and accurate technology that can detect counterfeit, adulterated or mis-labeled pharmaceuticals. If you want more information on this anti-counterfeiting solution, you can check it out at www.xstreamsystems.net or www.securepharmachain.com.
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XStream Systems produces pharmaceutical authentication solutions. Their patented systems are based on Energy-Dispersive X-Ray Diffraction (EDXRD) technology. The company’s XT250™ System enables testing of powders, pills AND entire sealed bottles