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<p>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.</p>
<p>This Standard does not apply to in vitro diagnostic medical devices.</p>
Reģistrācijas numurs (WIID)
32217
Darbības sfēra
<p>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.</p>
<p>This Standard does not apply to in vitro diagnostic medical devices.</p>
