BEGIN:VCALENDAR
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;VALUE=DATE:20241008
DTEND;VALUE=DATE:20241010
DTSTAMP:20260727T001742
CREATED:20240311T100835Z
LAST-MODIFIED:20240311T100835Z
UID:17696-1728345600-1728518399@globalregulatorypress.com
SUMMARY:Design Controls for Medical Devices and IVDs
DESCRIPTION:This two-day course covers design control principles\, and design and development regulatory requirements according to the US 21 CFR Part 820\, ISO 13485:2016 and the EU MDR. Practical examples will be incorporated. The course covers important requirements for medical device and IVD design controls. Learners will benefit from open dialogue and the sharing of current design and development processes; highlighting how misperceptions of regulatory requirements have led to less-than-optimal practices. This course also provides guidance for all phases of medical device design and development projects\, as well as retrospective gap analysis of design history files to help develop new technical files under the EU MDR and IVDR. \nOrganiser: NSF \nLocation: Virtual \nContact: https://www.nsf.org/training/series/design-controls-for-medical-devices-and-ivds-training \n
URL:https://globalregulatorypress.com/event/design-controls-for-medical-devices-and-ivds-2/
ATTACH;FMTTYPE=image/png:https://globalregulatorypress.com/wp-content/uploads/2022/01/webinar.png
END:VEVENT
END:VCALENDAR