Automating Day To Day Fda Compliance In 20 Global Medical Manufacturing Facilities – Advanced Manufacturing Systems

  • How equipment connectivity to MES “forces” day to day regulatory compliance
  • Case study will cover global I.T. systems for 20 medical factories with 500+ production lines, shipping 35M+ top level assemblies per year
  • Medical production lines range from those producing highly complex instruments to high volume “lights out” production lines
  • Discussion of UDI and GAMP5 Compliance Requirements.

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