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DTSTART;TZID=Europe/London:20230209T100000
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DTSTAMP:20260407T202140
CREATED:20221216T083732Z
LAST-MODIFIED:20230203T114611Z
UID:21607-1675936800-1675940400@staging.medilinkmidlands.com
SUMMARY:Beginner's Guide to developing and releasing a new Medical Device or IVD
DESCRIPTION:  \n  \n  \nThis free-to-attend event is part of the West Midlands Academic Health Science Network (WMAHSN) industry event programme\, aimed to support the West Midlands innovation ecosystem\, and to make the West Midlands healthier\, more productive and deliver the best possible clinical outcomes for patients. \nMedical devices and IVDs are a highly regulated industry\, and the regulatory considerations should be considered at the earliest stages of your strategic planning to help ensure that your products can be successfully approved and commercialised. \nThe webinar will provide a high level overview of the critical considerations and overview of the key steps needed from initial planning through to successfully selling the product after regulatory approval. \nThe webinar will cover the following focus areas; \n\nRegulatory planning as part of your product get-to-market strategy\nConsiderations for product design and development\nNavigating the regulatory approval process\nCommercial launch and beyond – demonstrating continuing safety\, performance and compliance to keep your product approval.\n\n CLICK HERE TO SECURE YOUR PLACE\nTarget audience \n\nThis webinar training session is aimed at companies looking to or currently developing a new medical device and explores the critical strategic\, operational and industry specific considerations necessary for successful commercialisation of a medical device or IVD product\, with a focus on the regulatory and legal compliance environment.\nThis webinar is aimed at business leaders\, product developers\, software developers\, technical managers\, quality and regulatory professionals.\n\n  \nTimothy Bubb\, Technical Director\, IMed Consultancy \nTim Bubb is a Principal Consultant and heads up the medical device consulting team at IMed Consultancy. Tim specialises in high-risk active therapeutic medical devices\, software\, digital health\, and AI/ Machine learning\, such as defibrillators\, ventilators\, and clinical decision support software. Tim has a wealth of experience in medical device quality\, regulatory\, clinical\, and design engineering fields\, having held senior industry positions in both multinational and SME manufacturers with overall responsibility for ensuring product legal compliance from concept through to regulatory approval\, and successful commercialisation. \nIMed Consultancy is a Medical Device and IVD specialist Regulatory and Quality consulting company\, helping manufacturers achieve and maintain regulatory approvals for their products and quality management systems through a variety of consulting and representation services. \n 
URL:https://staging.medilinkmidlands.com/event/beginners-guide-to-developing-and-releasing-a-new-medical-device-or-ivd/
LOCATION:Online
CATEGORIES:Medilink Midlands Event
ORGANIZER;CN="Medilink Midlands":MAILTO:zoeh@medilinkwm.co.uk
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