An NSF International Company M3 - CE & Global Clinical Requirements - Planning and Conducting Clinical Investigations for Medical Devices
PrintPart of Medical Devices QP Training Module 3
£735.00 exl VAT
About this course
From establishing what should be within the clinical study protocol to understanding the actual stages for applying for Clinical Investigation with European Competent authorities, this course will enable you to understand the decision making and practical aspects concerning EU Clinical Investigations.
Who Should Attend
Development, regulatory and clinical personnel involved in the formulation of clinical investigations, evaluations and post market clinical follow-up of medical devices. The medical devices requirements are placing a major emphasis upon clinical data requirements for devices, therefore programme managers, marketing and senior managers will also benefit from this module in that they will be able to understand the clinical requirements necessary for their devices and plan an appropriate commercialization strategy.
