Global Medical Device Reporting - A Comparison of Worldwide Regulations 2013

  • 22 Mar 2013
  • Webinar

Description

The Global Medical Device Reporting - A Comparison of Worldwide Regulations 2013 is a webinar that covers topics such as:

  • Medical Device Vigilance
  • Edical Device Reporting
  • Serious injury
  • Malfunction
  • Who Reports
  • Incident
  • Timing requirements
  • Decision Trees – when to report
  • Regulatory agencies next steps
  • Comparison of format of reports
  • Similar products
  • Capital equipment
  • Social Media
  • Maude Database
  • Alternative Summary Report (ASR)
  • EMDR
  • Remedial Action Exemption (RAR)

The Global Medical Device Reporting - A Comparison of Worldwide Regulations 2013 brings together:

  • Medical Device Regulatory affairs professionals
  • Medical Device Quality professionals involved in post market surveillance activities
  • Consultants in the global medical device regulatory space
  • Medical Device Quality Managers / Quality Directors / Quality VPs
  • Auditors
  • Medical Device Quality Engineers / Quality Assurance Professionals

Past Events

Important

Please, check "Global Medical Device Reporting - A Comparison of Worldwide Regulations" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Pharma
Technology: Biotechnology

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