Posts Tagged ‘FDA Compliance’

MAXLife Software for Medical Device Manufacturers

Thursday, May 6th, 2010

An end-to-end ERP application, MAXLife integrates planning and manufacturing processes with order management to provide available-to-promise and capable-to-promise processing, fully-integrated quality testing and quality control, online quoting and conversion to orders, kitting and assembly, lot and serial number traceability, and warranty and recall management. MAXLife is a powerful, yet flexible, business software solution that provides the scalability you need to grow your company profitably while producing the safest products possible. With MAXLife, Medical Device manufacturers can streamline their most common business process needs, including:

  • Lot Traceability
  • FDA 21 CFR Part 11 Compliance
  • Inventory Management
  • Improved Visibility
  • Lead Time Improvement
  • Waste Reduction
  • … and more!

Efficient Discrete Manufacturing

Designed for mid-size and larger companies, MAXLife is a global, multi-language, and multicurrency enterprise resource planning solution designed with medical device manufacturers in mind. Its core strengths are in manufacturing, order processing, and distribution, but includes applications for financials, CRM, SCM, human resources, project management and analytics. Because Microsoft Dynamics AX integrates with widely-familiar Microsoft products such as Microsoft SQL Server, BizTalk Server, Exchange, Office, and Window, employees can work with the tools they are likely to be already familiar with, lowering training costs.

FDA Compliance

MAXLife helps Medical Device companies demonstrate that they meet the processing, safety and tracking standards required by law. The software, documentation and services provided by Merit Solutions can help reduce the time and effort required to maintain FDA compliance by capturing and maintaining product information from each manufacturer.

Learn more about Life Sciences Software for Microsoft Dynamics AX.

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