Bringing Compliance To Design Control For Older Products 2013

  • 14 Nov 2013
  • Webinar

Description

Topics
  • Set procedures and template to complete remediation for design history file of old products to meet the new standards
  • Multi-functional team approach/responsibility
  • Gathering of data to build the design history files
  • Gap analysis
  • Risk assessment for prioritizing remediation
  • Risk procedure
  • Validations
  • Traceability matrix
  • Check list
  • Dealing with the FDA
Who should Attend
  • R&D and product development engineers and managers
  • End-users responsible for design control and technical files that need to be updated to the new standards
  • QA, Regulatory Affairs and team members who contribute to design history or technical files
  • Remediation teams
  • Consultants
  • Validation specialists
  • Corporate auditors

Past Events

Important

Please, check "Bringing Compliance To Design Control For Older Products" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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