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TZID:America/New_York
X-LIC-LOCATION:America/New_York
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TZNAME:EDT
DTSTART:19700308T020000
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UID:2140535:Event:67470
DTSTAMP:20260531T173849Z
SUMMARY:Webinar: Simplifying the Clinical Trial Regulatory Submission 
 Process
DESCRIPTION:The convergence of technologies in the clinical trials spa
 ce is improving efficiencies on all fronts of the clinical research pr
 ocess. Direct work with a focus group composed of representatives from
  many walks of the industry have led our group to the conclusion that 
 a source of difficulty largely unmitigated by available technologies t
 oday is the regulatory document tracking and submission process.\nUnde
 r the guidance of this group this webinar will explore the ways in whi
 ch a unified Clinical Trial Management System (CTMS) can deliver effic
 iencies across an enterprise of clinical development. Pulling the regu
 latory submission process into a software platform that has truly unfe
 ttered access to its data allows for powerful reporting, elimination o
 f redundant tasks, and the reduction of risk due to human error.\nLear
 n more about the webinar, \"Simplifying the Clinical Trial Regulatory 
 Submission Process\" \n\nFor more information visit https://medtechiq
 .ning.com/events/webinar-simplifying-the-clinical-trial-regulatory-sub
 mission
DTSTART;TZID=America/New_York:20151209T110000
DTEND;TZID=America/New_York:20151209T120000
CATEGORIES:free, webinar
LOCATION:Online
WEBSITE:http://xtalks.com/clinical-trial-regulatory-submission-process
 .ashx
URL:http://xtalks.com/clinical-trial-regulatory-submission-process.ash
 x
CONTACT:416-977-6555
ORGANIZER:Xtalks Life Science Webinars
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562013381?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Xtalks L
 ife Science Webinars":https://medtechiq.ning.com/profile/Xtalks
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