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VERSION:2.0
PRODID:-//Journal of Medical Device Regulation - ECPv4.9.3.2//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Journal of Medical Device Regulation
X-ORIGINAL-URL:https://globalregulatorypress.com
X-WR-CALDESC:Events for Journal of Medical Device Regulation
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20240508T130000
DTEND;TZID=Europe/London:20240508T170000
DTSTAMP:20260725T191734
CREATED:20240328T092617Z
LAST-MODIFIED:20240328T092617Z
UID:17756-1715173200-1715187600@globalregulatorypress.com
SUMMARY:MHRA MANUFACTURER'S ON-LINE REPORTING ENVIRONMENT (MORE) PLATFORM
DESCRIPTION:This webinar offers practical insight into the UK MHRA’s Manufacturer’s On-line Reporting Environment (MORE) platform. It will provide in-depth guidance on how to answer certain elements\, covering all forms of incident and other reports which must be notified by manufacturers to the MHRA in the event of an alleged adverse incident involving a medical device. Special notification\, for example originating at market surveillance\, will also be covered. Dedicated e-learning modules are presented on manufacturer’s incident reports\, market interventions by manufacturers and other topics. \nOrganiser: Quality First International \nLocation: Online webinar \nRegister: https://www.qualityfirstint.com/online-webinar \n
URL:https://globalregulatorypress.com/event/mhra-manufacturers-on-line-reporting-environment-more-platform/
ATTACH;FMTTYPE=image/png:https://globalregulatorypress.com/wp-content/uploads/2024/03/MOREwebinar-image.png
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