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DTSTART;TZID=Europe/London:20161117T080000
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UID:17625-1479369600-1479402000@staging.medilinkmidlands.com
SUMMARY:PMS and Periodic Safety Reports for MedTech & IVD Manufacturers
DESCRIPTION:Manufacturers of both Medical Devices and In Vitro Diagnostic products will be experiencing significant increases in expectations regarding clinical evidence and PMS. It is imperative that organisations plan now to ensure data is continually gathered\, analysed and reported to comply with these new regulations. \nMedilink WM\, in conjunction with Acclaim Biomedical Consulting\, is offering a one day workshop exploring the new requirements for increased PMS. With over 20 years experience in Medical Devices and IVDs\, Acclaim Biomedical Consulting are best placed to support and advise on the increased regulatory requirements and the impact these will have on existing practice. \nThe MPD Training course is designed to review critical elements of the new regulations and will be run as an interactive 1 day course designed for those with a good working knowledge of current requirements. \nWho should Attend \n  \n\nMedical Device Manufacturers\nIVD Manufacturers\nClinical Leaders\nRegulatory Affairs Officers and Managers\nQuality Control Officers and Managers\n\nDelegate Fees \nMember: £140 + VAT\nNon-Member: £190 + VAT \nTo find out more information or register your place\, please click here.
URL:https://staging.medilinkmidlands.com/event/pms-and-periodic-safety-reports-for-medtech-ivd-manufacturers/
LOCATION:MTIC\, 4 Greenfield Crescent\, Birmingham\, B15 3BE
ORGANIZER;CN="Sarah Wootton":MAILTO:sarahw@medilinkwm.co.uk
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