ISO 14155 2011.12
ISO 14155:2011 addresses good clinical practice for the design, conduct, recording and reporting of clinical investigations carried out in human .
ISO 14155-2-2 . 6.12
A Guide to European Medical Device Trials and BS EN ISO 14155 Duncan Fatz This is a sample chapter from A Guide to European Medical Device Trials and BS EN ISO 14155.
ISO 14155:2011 specifies general requirements intended to protect the rights, safety and well-being of human subjects, ensure the scientific conduct of the clinical investigation and the
Godkendelsesdato: 2012-12-21. Internationale relationer: EN ISO 14155:2011 IDT ISO 14155:2011 IDT. ICS: 11.040.01 - Medicinsk udstyr.
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