Resumen
This part of EN ϲʿ 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.
Ciclo de vida
-
Anteriormente
Retiradaϲʿ 14155:1996
-
Ahora
-
Revisada por
Retiradaϲʿ 14155:2011
¿Tiene alguna duda?
Consulte nuestras Ayuda y asistencia
Atención al cliente
+41 22 749 08 88
Horario de asistencia:
De lunes a viernes - 09:00-12:00, 14:00-17:00 (UTC+1)