3.4.12 Instruction in the use of devices Estimated reading: 1 minute 20 views Authors Aim and purpose Umsetzung der gesetzlichen Anforderungen zur Einweisung in die Anwendung von Medizinprodukten Application Description of the procedure Risks Resources Material Time required Documentation Responsibility and qualification Notes and comments Applicable documents Validation documents Terms Attachments 3.4 Resources - Previous 3.4.11 Commissioning, device management Next - 3.4 Resources 3.4.13 Fault report, repair management
