Developing the Risk Management File 2017

  • 18 Oct 2017
  • Webinar

Description

Developing the Risk Management File 2017 is a webinar that covers topics such as:

  • Assignment of Responsibilities and Authorities and a valuable Tool to help Manage them
  • The scope of the Plan and its Relationship to the device Life-cycle
  • Criteria for risk Acceptability including Distinctions between the International and EU versions
  • Review of Risk Management Activities
  • The necessary Verification Activities (implementation and effectiveness) and how they can link to the QMS
  • Special cases of Risk Acceptability that can often reduce the Risk Management Workload
  • Collection, Review, Evaluation, and Action from Production and Post-Production Information Collection

Developing the Risk Management File 2017 is intended for medical device manufacturers including:

  • R&D Managers
  • Top Management
  • Project Managers
  • Risk Managers
  • Design Project Team Members
  • Risk Management Team Members
  • MDR Specialists
  • Complaint Specialists

Past Events

Important

Please, check "Developing the Risk Management File" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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