BEGIN:VCALENDAR
PRODID:NingEventWidget-v1
VERSION:2.0
METHOD:PUBLISH
BEGIN:VTIMEZONE
TZID:America/New_York
X-LIC-LOCATION:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:19700308T020000
RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:19701101T020000
RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
UID:2140535:Event:470990
DTSTAMP:20260605T223121Z
SUMMARY:Design Control for Medical Devices Including Verification/Vali
 dation
DESCRIPTION:Overview of design control for medical devices with and em
 phasis on verification and validation of design inputs. Webinar will c
 over basic regulations regarding verification/validation of inputs, tr
 ace of inputs to verification/validation and techniques including stat
 istics for proper verification/validation of design inputs.\n\nWhy Sho
 uld You Attend:\nIn the development of medical device, incomplete unde
 rstanding and implementation of design controls will lead to rejection
  of an application for approval by the FDA or rejection of a CE mark a
 pplication. Incomplete, improper or missing verification and validatio
 n is a cause of many products not being approved for market. This semi
 nar will give the participants the basics to be able to work through t
 he concepts of design verification/validation and implement these conc
 epts in their respective areas.\nVerification and validation of design
  inputs is a critical step in the development of medical devices. It i
 s the objective evidence that the developer developed what they set ou
 t to develop and the final product meets its design goals and needs of
  the end user. Without proper verification/validation of inputs, it is
  not possible to prove to regulatory agencies that you have a product 
 which is safe and effective and that it meets its design requirements.
 \nAreas Covered in the Webinar:\n\nOverview of design control flow and
  were verification and validation fit in\nBasic trace from inputs to v
 erification and validation\nMethods of verification and validation of 
 inputs including statistics\nWriting protocols and records\nDiscrepanc
 ies and deviations\nTrace matrices form inputs to outputs\n\nWho Will 
 Benefit:\nThis webinar is appropriate to anyone working in design, dev
 elopment, marketing or support of regulated medical devices. People wo
 rking in R&D, Quality Assurance, Validation, Regulatory Affairs, Marke
 ting, Production and Product Support will benefit from this informatio
 n.\n\nFor more information visit https://medtechiq.ning.com/events/des
 ign-control-for-medical-devices-including-verification
DTSTART;TZID=America/New_York:20220224T100000
DTEND;TZID=America/New_York:20220224T130000
CATEGORIES:webinar
LOCATION:online
WEBSITE:https://www.complianceonline.com/design-control-medical-device
 -verification-validation-webinar-training-706619-prdw?channel=MedTech%
 20I.Q
URL:https://www.complianceonline.com/design-control-medical-device-ver
 ification-validation-webinar-training-706619-prdw?channel=MedTech%20I.
 Q
CONTACT:8887172436
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/10061239856?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
END:VEVENT
END:VCALENDAR