RO
SR EN ISO 14155-1:2009
Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003)
ISO 14155-1:2002 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. ISO 14155-1:2002 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,specifies requirements for the organization, conduct, monitoring, data collection and documentation of the clinical investigation of a medical device,is applicable to all clinical investigation(s) of medical devices whose clinical performance and safety is being assessed in human subjects. ISO 14155-1:2002 i
Status :
Withdrawn
Approval date : 12/15/2009
Publish date : 12/17/2009
Withdrawal date : 7/29/2011
Number of pages : 30
ICS : 11.100.20 Biological evaluation of medical devices
Technical Committee : 377 - Medical devices
- Replaces SR EN ISO 14155-1:2003
- Normative reference SR EN ISO 14155-2:2009
- Replaced by SR EN ISO 14155:2011