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SUMMARY:Impact and Assessment of European Medical Device Regulations
DESCRIPTION:The Medical Devices Regulations are due for significant update with areas such as Post Market Surveillance and Economic Operators being major areas of change. The final form of the regulations is now set and due to be voted into European Law. \nThe new regulations need to be considered now at all organisational levels as they will be impacting on decisions made today. \nThis course is designed to review critical elements of the new regulations. This training course will be an interactive in-depth 1 day session. \nCourse Content and Key Topics \n  \n\nEconomic Operator Responsibilities\nClinical Evidence\nTechnical Documentation\nPost Market Requirements\nConformity Assessment and the Scrutiny Process\n\nLearning Objectives \nProvide attendees with the tools and insight to plan and implement their organisations strategy\, for continued access to the European Market by the deadlines set in the new regulations. \nTo have gained a better understanding of the new regulations and the impacts the new regulations will have. \nWho should attend? \nAnyone wanting to advance their current understanding of how medical device regulatory affairs work in the EU and what regulators expect. \nBusiness owners\, financiers and entrepreneurs working with medical devices companies are also likely to find this course interesting. \nDelegate Fees \nMembers: £140\nNon-Members: £190 \nTo register or find out more information please contact Vanessa Bailey by email or by calling 0121 452 5630. \n\n 
URL:https://staging.medilinkmidlands.com/event/impact-and-assessment-of-european-medical-device-regulations/
LOCATION:MedilinkWM\, 4 Greenfield Crescent\, Edgbaston\, West Midlands\, B15 3BE
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