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| Medical Device Safety |
| Medical devices when combined with prescription drugs are under constant scrutiny from both state and federal regulators to improve safety and compliance. All participants in the life sciences supply chain, including manufacturers, distributors, hospitals and clinics must constantly add capabilities to their systems and processes to meet the latest regulatory and legislative hurdles. |
 With rapid globalization and increasingly porous borders, the life sciences industries have also faced challenges from counterfeit products being introduced into the supply chain. As a result, new ePedigree laws have been enacted in over 30 states that require an authentic chain of custody for each medical device that includes a pharmaceutical product throughout the supply chain. These laws are particularly challenging because of the number of products that need to be tracked as well as differing requirements posed by different regulatory requirements from each state. |
| In addition, the medical device industry needs the ability to execute targeted recalls for defective product. In the past, this has been a monumental task to identify which products are affected and where they are located in the supply chain. |
| rfXcel offers a suite of products to assist manufacturers, distributors, hospitals and clinics in improving the safety and security of their products and supply chains. rfXcel offers an application to enable complete traceability of components and raw materials as well as finished goods traceability to the customer. In addition, rfXcel has an application to enable compliance with ePedigree laws. rfXcel solutions can provide compliance with state, federal and international regulations. |
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| © Copyright 2011 rfXcel - Safety through Traceability™. All Rights Reserved. |
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