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Tag: Medical Devices

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Tag Archive: Medical Devices

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Rebate Management: the “Secret” Ingredient for Driving Growth

Rebate programs are powerful tools for B2B companies in a broad swath of industries, particularly those where margins are tight and pricing strategies can make all the difference. When properly structured and implemented, they can establish market differentiators, create purchasing…

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Using Medical Device Manufacturing Software for UDI

Does your company manufacture products that need to comply with unique device identification (UDI) guidelines? If so, you may be able to use advanced software to better label and track your products. Sage X3 provides a flexible software solution aimed…

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3 Medical Device Manufacturing Trends

Medical device manufacturing is a fast-paced industry in which new products and updates are continually rolling out. While innovation is essential, so too are quality control, standardization, and compliance. Medical device manufacturers are charged with creating a fast and efficient…

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Sage X3: ERP Software for Pharmaceutical Manufacturers

There are several ERP systems on the market designed to address the specific challenges facing pharmaceutical manufacturers. When you’re a pharmaceutical manufacturer, however, it doesn’t always feel that way – it feels like you’ll never find the solution that’s right…

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An ERP System for Pharmaceutical Companies

Choosing the right cost effective pharmaceutical manufacturing enterprise resource planning (ERP) solution is necessary for any organization that wants to improve visibility, increase efficiency, reduce costs, and improve product quality. While organizations initiate ERP projects for a variety of reasons,…

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6 Ways Sage X3 Can Help Your UDI Implementation

To remain FDA compliant, all medical devices must have labels that contain a unique device identification (UDI) – a number that makes them recognizable and traceable across the entire medical field – by 2020. The UDI, readable by both humans…

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5 Things to Consider When Defining Your UDI Strategy

The FDA has passed legislation requiring all medical devices to have a unique device identification (UDI) number to make them recognizable and traceable across the entire medical field. By 2020, all medical devices must have labels containing the UDI, which…

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What You Need to Know About a UDI Implementation Strategy

In 2007, the government passed the Food and Drug Administration Amendments Act (FDAAA). This act required the Food and Drug Administration (FDA) to establish a unique device identification provision for the purpose of increasing patient safety by improving the handling…

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Is Your ERP System Keeping You Compliant?

Managing compliance requirements is a concern for a variety of industries, and remaining up to date with state and federal regulations demands continuous due diligence on the part of business executives. A properly designed and developed ERP system can assist…

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Medical Device Manufacturing Software System Requirements to Consider

The FDA, regulatory compliance requirements, challenging timetables, and strict quality assurance needs are only a few of the hurdles medical device companies face when searching for an enterprise resource planning (ERP) solution. Medical device companies frequently need to look beyond…

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