Full Description

This document addresses good clinical practice for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the clinical performance or effectiveness and safety of medical devices.

For post-market clinical investigations, the principles set forth in this document are intended to be followed as far as relevant, considering the nature of the clinical investigation (see Annex I).

Product Details

Published:

01/31/2025

ISBN(s):

9780539350593

Number of Pages:

108

File Size:

1 file , 3 MB

Note:

This product is restricted and cannot be purchased in the following countries Ukraine, Russia, Belarus