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DTSTART;TZID=Europe/London:20200304T120000
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DTSTAMP:20260423T140149
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SUMMARY:Are you an Innovator working in mHealth?
DESCRIPTION:Aimed to give developers clear guidance\, helping to get the right market with the right product\, fit for NHS and worldwide quality standards \nThe NHS and national health bodies across the world are revolutionising services through the integration of digital health solutions\, leading to more patient-centered and efficient care. Frameworks guide the identification of health apps that will safely make the biggest impact in terms of improving outcomes. \nAs a developer\, it can be hard to know what technical requirements and evaluation will be imperative\, and how to navigate the system to ensure the right people know about your innovation. \nThis half day workshop aims to give developers clear guidance\, helping to get the right market with the right product\, fit for NHS and worldwide quality standards. Industry experts will provide practical advice\, with useful tools to future proof your innovation and be business ready. \nYou will hear from: \n-ORCHA Co-Founder & COO\, Tim Andrews & ORCHA Associate Paul Davies\n-Wayne Shirt and Marcus Hinde from NHS Digital\n-Medilink West Midlands and real life case studies. \nCome and be part of the day\, to learn: \n-What the app accreditation landscape is across the UK\, EU and globally\n-Deep dive into the Medical Device Regulations and what this means for you and your product\n-mHealth Regulation and technical Safety – What are the current regulations and what new requirements are coming shortly for mhealth?\n-Real life examples on how and where are Apps being used in clinical practice today? And what are the barriers and opportunities to making mhealth part of what is done in everyday clinical practice?\n-Useful\, practical take away tools\n-Networking opportunities \nProgramme: \n12:00 – Arrival\, registration and networking lunch \n12:45 – Presentations commence \n15:00 – Refreshment break \n17:00 – Event concludes \nBooking information: \nTo secure your place please complete the online booking form. Invoices will be issued once registration is complete. If you have any queries please click here to contact Zoe Heather. \nMedilink member – £20+VAT / Non-member – £35+VAT \n 
URL:https://staging.medilinkmidlands.com/event/are-you-an-innovator-working-in-mhealth/
LOCATION:Kuehne+Nagel Ltd\, 3 Avenue Road\, Birmingham\, West Midlands\, B6 4DU
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="Zoe Heather":MAILTO:info@medilinkmidlands.com
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DTSTART;TZID=Europe/London:20200311T083000
DTEND;TZID=Europe/London:20200311T143000
DTSTAMP:20260423T140149
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SUMMARY:How to increase quality & manufacturing processes through digitisation
DESCRIPTION:Medilink WM and MasterControl invite you to attend a free workshop to learn more about the changing medical device regulatory environments\, successfully navigating audits and the value of using digital solutions for managing quality and compliance. Offering attendees a better understanding of ‘How to be nimble in an ever-changing regulatory environment and easily manage the audit process with digitisation.’ \nHighly-knowledgeable life sciences industry experts will provide valuable insight on these topics and demonstrate how medical device and component manufacturers can position themselves for success. \nYou will hear from industry experts including Stephen Turnock\, Global Sales Director EMEA\, MasterControl and guest speaker Matthew Theobald\, Three Circles who will cover: \n\nMedical Device Audit Fundamentals\, MD SAP including the regulatory impact on audits\nAssessing your company’s current readiness for implementing a quality platform\, (MasterControl EBR)\nAn overview of the regulatory and quality management system requirements for a concept medical device\, understand the technical document that should be in place and explore risk management.\nImprove Product Quality & Operational Efficiency with Paperless Processes\n\nAttendees also have the opportunity to a private tour of the MTC facility. \nThis workshop will include opportunities to network and learn from your peers about their best practices and use of technology to navigate regulatory pathways and achieve compliance.
URL:https://staging.medilinkmidlands.com/event/how-to-increase-quality-manufacturing-processes-through-digitisation/
LOCATION:The MTC\, Ansty Park\, Coventry\, CV7 9JU
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="Zoe Heather":MAILTO:info@medilinkmidlands.com
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DTSTART;TZID=Europe/London:20200331T103000
DTEND;TZID=Europe/London:20200331T154500
DTSTAMP:20260423T140149
CREATED:20200207T133917Z
LAST-MODIFIED:20200207T133917Z
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SUMMARY:Software/AI Medical Device EU MDR CE Marking Workshop
DESCRIPTION:SEHTA and Psephos Biomedica next workshop is on Software / AI Medical Device EU MDR CE Marking. \nWhy attend? \nThere has been an explosion of software health technologies applying algorithms and artificial intelligence to address medical needs\, furthermore many traditional devices are adding software components or becoming digital. \nIn order to make these medical technologies available in Europe\, they must be CE marked which is currently governed by the Medical Device Directive and will be replaced in May 2020  by the new EU Medical Device Regulations (2017/745 & 746). \nDate:  Wednesday 31st March 2020 \nVenue:  Hill Dickinson\, Broadgate Tower\, 20 Primrose Street\, London EC2A 2EW \nTime:  10:30 – 15:45 \nCost:  SEHTA members fee: £270 + VAT / Non-Members: £320 + VAT per delegate \nNot a member of SEHTA?  It’s free to join – just click here \nFor more information and to register please click here
URL:https://staging.medilinkmidlands.com/event/software-ai-medical-device-eu-mdr-ce-marking-workshop/
LOCATION:Hill Dickinson\, Broadgate Tower\, 20 Primrose Street\, London\, EC2A 2EW
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="SEHTA":MAILTO:info@sehta.co.uk
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