Uncovering and Managing Successful Post Market Compliance for Medical Devices

Description

Uncovering and Managing Successful Post Market Compliance for Medical Devices is a conference that covers topics such as:

  • Firms MDR reporting and FDA`s handling of MDR reports
  • How to comply with complicated Compliant Handling, MDR and Recall requirements
  • Risk of regulatory enforcement actions
  • Company preparation in the event of a Recall, recall strategy, notification letter and communicating with the FDA
  • Relationship and interaction with other quality system elements as they relate to complaints and reportable events
  • Creation and maintenance of effective procedures for handling complaints, reportable events and recalls
  • Designing Standard Operating Systems for communicating process for firm`s success
  • Case examples
  • FDA`s New Guidance`s on Risk and how it interacts with Recalls

Uncovering and Managing Successful Post Market Compliance for Medical Devices brings together attendees from:

  • QA/QC
  • Regulatory Affairs
  • Regulatory Professional
  • Project Managers
  • Complaint Handling Teams
  • Risk Managers
  • CAPA Teams

Future Events

Uncovering and Managing Successful Post Market Compliance for Medical Devices 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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