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SUMMARY:MPD Training Course: European Union Intermediate/Advanced Regulatory Affairs for Medical Devices
DESCRIPTION:Medilink East Midlands\, together with Medical Device Consultancy (MDC) are offering a one day training course which will provide delegates with an intermediate to advanced understanding of regulatory affairs for Medical Devices in the European Union. \nThis course will provide answers and practical methods by answering the following questions: \n\nDo you use the ‘Blue Guide’? What is it and why is it important?\nWhat matters more: Best practice\, regulations or legal requirements\, and why?\nDo you know how to determine the ‘Direction of Travel’ for medical device regulation?\nWhat else does a CE mark really mean?\nDoes usability really matter? What is ‘Human Factors Engineering’?\nHow do you handle software? Are you compliant?\nHow do you undertake clinical evaluations and investigations that make a difference?\nWhat is in the proposed new Regulations and what matters to you?\n\nBy attending this course you will improve your day-to-day management of regulatory affairs\, learn about the changes to roles and responsibilities of key stakeholders and understand where to find and use guidance that helps you achieve full compliance. \nTo view the programme and further information click on the Event Brochure PDF below.\n \nTo register your place\, please complete the ‘Book Online Now’ form below. 
URL:https://staging.medilinkmidlands.com/event/mpd-training-course-european-union-intermediateadvanced-regulatory-affairs-for-medical-devices/
LOCATION:Best Western Premier Yew Lodge Hotel\, 33 Packington Hill\, Kegworth\, Derby\, DE74 2DF\, United Kingdom
ORGANIZER;CN="Becky Brown":MAILTO:info@medilinkem.com
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