Unique Device Identification (UDI) Final Rules Overview 2013

  • 06 Nov 2013
  • Webinar

Description

Unique Device Identification (UDI) Final Rules Overview 2013 is a webinar that covers topics such as:

  • Definitions
  • Applicable Statute(S), Regulations and Enforcement Authority
  • UDI Final Rules: Technical Requirements and Changes Made
  • UDI Development History
  • UDI System Requirements including Technical Standards
  • When to Use a UDI and When to Discontinue Its Use
  • FDA Accreditation Process for an Issuing Agency including Suspension and Revocation
  • Requirements for a Unique Device Identifier
  • UDI Rules: Exceptions and Alternatives
  • UDI Rules: Applicability
  • Device Identifier Formats including Dates
  • Compliance Dates for the Applicable Requirements Over Seven (7) Years
  • Impact of the Final Rules to Many Business Areas/Processes
  • Global UDI Database (GUDID): Technical Requirements (Data Format and Data Attributes)
  • Practical, Actionable, and Sustainable Strategy: Good Practices to Implement UDI Systems Fast
  • Changes in Device Design, Documentation and Manufacturing Processes
  • Conclusion

Unique Device Identification (UDI) Final Rules Overview 2013 is intended for:

  • Regulatory Affairs and Compliance Professionals
  • R&D Scientists, Managers, Directors, and VPs
  • Quality Professionals
  • Clinical Affairs Professionals
  • Legal and Compliance Officers
  • Consultants
  • Senior Management
  • Marketing Professionals
  • Anyone Interested in the Subject

Past Events

Important

Please, check "Unique Device Identification (UDI) Final Rules Overview" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Internal Audit & Compliance, Quality assurance, Risk Management
Education: Training
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Medical technology
Industry: Food & Beverages

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