BS EN ISO 14155-1:2009 defines procedures for the conduct and performance of clinical investigations of medical devices. It specifies general requirements intended to

- protect human subjects,

- ensure the scientific conduct of the clinical investigation,

- assist sponsors, monitors, investigators, ethics committees, regulatory authorities and bodies involved in the conformity assessment of medical devices.

This part of BS EN ISO 14155-1:2009

a) specifies requirements for the conduct of a clinical investigation such that it establishes the performance of the medical device during the clinical investigation intended to mimic normal clinical use, reveals adverse events under normal conditions of use, and permits assessment of the acceptable risks having regard to the intended performance of the medical device,

b) specifies requirements for the organization, conduct, monitoring, data collection and documentation of the clinical investigation of a medical device,

c) is applicable to all clinical investigation(s) of medical devices whose clinical performance and safety is being assessed in human subjects.

BS EN ISO 14155-1:2009 is not applicable to in vitro diagnostic medical devices.



Cross References:
ISO 14155-2
ISO 14971
ISO 10993
93/42/EEC
90/385/EEC


All current amendments available at time of purchase are included with the purchase of this document.