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Norm

ÖNORM EN ISO 14155-1

Issue date: 2009 12 01

Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003)

This part of ISO 14155 specifies requirements for the conduct of a clinical investigation such that it establishes the performance of the medical device during the clini...
Withdrawn: 2011 05 15
§ Legal References
Publisher:
Austrian Standards International
Format:
Digital | 31 Pages
Language:
German | English
Optionally co-design standards:
This part of ISO 14155 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. It specifies requirements for the organization, conduct, monitoring, data collection and documentation of the clinical investigation of a medical device and is applicable to all clinical investigation(s) of medical devices whose clinical performance and safety is being assessed in human subjects.
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Clinical investigation of medical devices for human subjects — Part 1: General requirements