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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:20220215T080000
DTEND;TZID=Europe/London:20220216T170000
DTSTAMP:20260727T001623
CREATED:20211112T104459Z
LAST-MODIFIED:20211112T104459Z
UID:14178-1644912000-1645030800@globalregulatorypress.com
SUMMARY:Software as a Medical Device
DESCRIPTION:Location: Hilton Rotterdam\, The Netherlands \nDescription: The unique challenges faced in earning approval for medical software products require a different approach from other medical devices. In addition\, cybersecurity concerns and the rise of artificial intelligence bring new regulations and guidance documents published on a weekly basis. This in-person even will look at the history and current state of play of software as a medical device (SaMD). Global requirements will be discussed\, including the EU and US regulations\, along with: \n\nHow to determine when software is considered regulated as SaMD\nHow to determine the correct class/classifications under global requirements\nSoftware lifecycle management and performing risk assessment.\n\nIn addition\, practical case studies will be presented for each subject. \nOrganiser: RAPS \nContact: https://www.raps.org/events/software-as-a-medical-device-02-2022 \n
URL:https://globalregulatorypress.com/event/software-as-a-medical-device/
ATTACH;FMTTYPE=image/jpeg:https://globalregulatorypress.com/wp-content/uploads/2020/11/software.jpg
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