Standard
ISO 14155-2:2003
[Superseded]Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
This part of EN ISO 14155 provides requirements for the preparation of a Clinical Investigation Plan (CIP) for the clinical investigation of medical devices. The compilation of a CIP in accordance with the requirements of this standard and adherence to it will help in optimising the scientific validity and reproducibility of the results of a clinical investigation.
This Standard does not apply to in vitro diagnostic medical devices.
Published: 16/05/2003
Pages: 9
Content history
One-time Purchase
Access via web browser on any device
One-time purchase
Single publication
Offline access via PDF^
$122.50 AUD
Inclusive of GSTFormat *
Web Reader (PDF)
Licenses *
1 user
Total$122.50 AUD
IMPORTANT