Presented as a virtual conference via a web cast.  

About the Conference

“The word ‘risk’ is thrown at me from a lot of different directions, with a lot of different definitions.  How do I deal with it?”

Sound familiar?

New regulations, standards, and concepts of risk add complexity and offer opportunities to medical product manufacturers.  Beyond the challenge of dealing with differing definitions and expectations, companies wrestle with the practical application risk and benefit-risk concepts and tools throughout the product life cycle. 

Run by recognized risk experts in the med tech field, this conference focuses on the practical understanding and application of current risk management principles and tools for manufacturers of medical devices, diagnostics, and combination products.


Who should attend:

  • Risk management
  • Compliance
  • Executive management
  • R&D
  • Regulatory affairs
  • Quality assurance
  • Supply chain management
  • Software
  • Medical / patient safety


What you will learn:

  • The efficient and effective application of risk management concepts and tools
  • Trends in medical product risk management
  • New US and global risk management regulations and standards
  • Determining risk acceptability
  • The practical determination and use of “benefit”
  • End user perspectives on risk
  • Maturity models ane the Pre-Cert program
  • Addressing residual risk
  • Risk management with connected devices
  • Enterprise risk management
  • Remediation of legacy product risk files
  • Diagnostics risk management
  • Software risk management
  • Combination product risk management


CEU Information

Attendees can earn CEUs. 1 hour of the conference = 1 CEU. MedTech Intelligence will provide you a Certificate of Attendance with the amount of CEU's earned about three weeks after the conference.

MTI's conference CEUs can be applied to your Regulatory Affairs Certification.


  • When

  • Tuesday, March 6, 2018 - Wednesday, March 7, 2018
    8:30 AM - 4:00 PM

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