UDI Implementation 2015

  • 15 Apr 2015
  • Webinar

Description

UDI Implementation 2015 is a webinar that covers topics such as:

  • The three locations for UDI: direct marking, labeling, and packaging
  • Distinguishing among identification, tracking, and tracing
  • The UDI form including the required elements and the optional elements
  • When a UDI is required, including the exceptions
  • When a new version of a model requires a new UDI
  • The data elements required for FDA’s global database (GUDID)
  • Implications for FDA inspections
  • Changes required in the Quality Management System including QSR, MDRs, etc

UDI Implementation 2015 is intended for:

  • Design engineers
  • Regulatory managers
  • Project managers
  • Labeling specialists
  • Quality engineers
  • Quality managers
  • Complaint handling and MDR specialists

Past Events

Important

Please, check "UDI Implementation" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma
Industry: Food & Beverages
Science: Life Sciences & Biology

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