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Clinical Research Organization

ISO 14155 Third Edition Preview: Role of Risk Management in Clinical Investigations

EMERGO SUMMARY OF KEY POINTS:

  • The anticipated update to ISO 14155 in 2019 includes stronger requirements for clinical risk management.
  • The third edition of the ISO 14155 medical device clinical investigation standard will align more closely to ISO 14971 medical device risk management concepts.
  • Quality management principles applied to clinical investigation audits are also introduced in ISO 14155’s latest edition.

No Shortcuts: Building Out the Right Processes to Ensure Medical Device Safety and Security

EMERGO BY UL SUMMARY OF KEY POINTS:

  • Regulatory focus on medical device safety and risk management intensifying;
  • Functions such as clinical research, post-market surveillance and ISO 14971 compliance should bolster safety and risk management efforts;
  • More robust safety and risk management processes to help medical device companies pivot faster when regulators change requirements.