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DTSTART;TZID=Europe/London:20230420T140000
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DTSTAMP:20260415T133249
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SUMMARY:WEBINAR: SEHTA & Psephos Biomedica Taster: MHRA Clinical Investigations: Best Practice and Future Insights
DESCRIPTION:               \n\n\n\nSEHTA’s MDR Regularory Partner Psephos Biomedica are delighted to bring you this FREE to attend taster webinar session on MHRA Clinical Investigations to help you get up to to date on the latest developments and understand the approval process plus future insights.\n\n\n\nCLICK HERE TO BOOK YOUR FREE PLACE TODAY\n\nSpeaker Profiles\n  \n \nRobin Stephens\, CEO & Co-Founder\, Psephos Biomedica \nPresentation Title: Insights into the future at MHRA / in the UK \n \nMark Grumbridge\, Head of Clinical Investigations\, MHRA \nPresentation Title: Clinical investigations – approval process and best practice \n\n\n\n\n\n\n\n\n\n\n\nWhy attend?\nThe UK has always fostered a clinical research friendly environment aiming to advance disease diagnosis\, medical therapies and improved patient care. With an increasing interest in medtech clinical investigations this webinar will provide an overview of the UK Medicines and Health products Regulatory Agency (MHRA) process for research clearance\, advice and support. If you are involved in clinical investigations in the UK at any level this informative webinar is for you. \nWho should attend?\nClinical research staff (VP\, Director\, Manager\, Specialist\, Associate); medtech entrepreneurs; regulatory staff (VP\, Director\, Manager\, Specialist\, Associate); anyone interested in the future of medtech clinical research in the UK.\n\n\n\n\n\n\n\n  \n 
URL:https://staging.medilinkmidlands.com/event/webinar-sehta-psephos-biomedica-taster-mhra-clinical-investigations-best-practice-and-future-insights/
CATEGORIES:Medilink Partner Event
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DTSTART;TZID=Europe/London:20230426T100000
DTEND;TZID=Europe/London:20230426T110000
DTSTAMP:20260415T133249
CREATED:20230323T133712Z
LAST-MODIFIED:20230323T134434Z
UID:22817-1682503200-1682506800@staging.medilinkmidlands.com
SUMMARY:WEBINAR: SEHTA & IVDeology Taster: The UKCA Mark: Are you ready?
DESCRIPTION:SEHTA and IVDeology\, a leading regulatory company specifically within the in vitro diagnostic medical device industry\, are delighted to offer this webinar to start-up companies who are looking to place devices on the UK market. \nThe session will be delivered by Nancy Consterdine\, Director of Training and Compliance Services at IVDeology and will cover the following: \n Programme \n10:00 – 10:05 – Welcome & Introduction \n10:05 – 10:50 – Main presentation \n\nThe current requirements for placing devices on GB and NI markets – the clock is ticking\nThe role of the UK Representative and what to look for when appointing one\nThe best estimate of future requirements as directed by the consultation outcomes and recent MHRA communications including the role of the Qualified Person and transition timelines\n\n10:50 – 11:00 – Q&A \n11:00 – Close \nCLICK HERE TO BOOK YOUR FREE PLACE TODAY
URL:https://staging.medilinkmidlands.com/event/webinar-sehta-ivdeology-taster-the-ukca-mark-are-you-ready/
LOCATION:Online
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="SEHTA":MAILTO:info@sehta.co.uk
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