Managing Your Medical Device Reporting (MDR)Program for Compliance Success 2012

  • 29 Nov 2012
  • Webinar

Description

Managing Your Medical Device Reporting (MDR)Program for Compliance Success 2012 is a webinar that covers topics such as:

  • Reporting device-related deaths and serious injuries and when these are not treated as a product complaint
  • How will I know if I require more information about my medical device report?
  • Are there exemptions, variances, or alternative forms of adverse event reporting requirements?
  • The manufacturer`s reporting requirements and expectations
  • Develop, maintain, and implement written MDR procedures and achieve compliance
  • Learn what constitutes a MDR and how to facilitate this for compliance success
  • Learn why FDA is amending its MDR regulations to remove a requirement for baseline reports that the agency deems no longer necessary

Managing Your Medical Device Reporting (MDR)Program for Compliance Success 2012 brings together:

  • Regulatory Affairs and Compliance
  • QA/QC
  • Consultants
  • Engineering/Technical Services/Operations

Past Events

Important

Please, check "Managing Your Medical Device Reporting (MDR)Program for Compliance Success" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Medical laboratories, Medical technology, Pharma

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