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EU Medical Device Directive: Part I - Introduction (Korean) v2

This training intends to provide basic information concerning the European Medical Device Directive and the CE marking of medical devices.
€78,96

ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials (Chinese)

ISO 14155 is intended to be applied worldwide to clinical investigations of medical devices in order to fulfill the various national, regional, and international regulatory requirements. In this course, the learner will be able to identify the specific requirements of ISO 14155. The learner will also be able to recognize the roles and responsibilities of sponsors and monitors in clinical investigations.
€78,96

ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials (Japanese)

ISO 14155 is intended to be applied worldwide to clinical investigations of medical devices in order to fulfill the various national, regional, and international regulatory requirements. In this course, the learner will be able to identify the specific requirements of ISO 14155. The learner will also be able to recognize the roles and responsibilities of sponsors a
€78,96

ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials (Korean)

ISO 14155 is intended to be applied worldwide to clinical investigations of medical devices in order to fulfill the various national, regional, and international regulatory requirements. In this course, the learner will be able to identify the specific requirements of ISO 14155. The learner will also be able to recognize the roles and responsibilities of sponsors and monitors in clinical investigations.
€78,96