BEGIN:VCALENDAR PRODID:-//Microsoft Corporation//Outlook 16.0 MIMEDIR//EN VERSION:2.0 METHOD:PUBLISH X-MS-OLK-FORCEINSPECTOROPEN:TRUE BEGIN:VTIMEZONE TZID:Eastern Standard Time BEGIN:STANDARD DTSTART:16011104T020000 RRULE:FREQ=YEARLY;BYDAY=1SU;BYMONTH=11 TZOFFSETFROM:-0400 TZOFFSETTO:-0500 END:STANDARD BEGIN:DAYLIGHT DTSTART:16010311T020000 RRULE:FREQ=YEARLY;BYDAY=2SU;BYMONTH=3 TZOFFSETFROM:-0500 TZOFFSETTO:-0400 END:DAYLIGHT END:VTIMEZONE BEGIN:VEVENT CLASS:PUBLIC CREATED:20220113T224244Z DESCRIPTION:Date/Time: March 01\, 2022 (Tuesday)\, from 1 – 2 pm ET\n \nB ackground:\nThe U.S. Food and Drug Administration (FDA)\, Center for Devic es and Radiological Health (CDRH)\, will host a public webinar about the F inal Guidance “Principles for Selecting\, Developing\, Modifying\, and A dapting Patient-Reported Outcome Instruments for Use In Medical Device Eva luation.”\n \nDuring this webinar\, the FDA will provide highlights of t he final guidance and answer questions from webinar attendees.\n \n \nWebi nar Connection Details\nWe encourage you to join at least 15 minutes prior to the start of the webinar. You do not need to register to attend. We re commend you join using the Zoom link below\, if possible:\n \n* Webinar Li nk: https://fda.zoomgov.com/j/1614531941?pwd=VC91aUFVeW5kSURnZC9jR1VXWmo4U T09\n* Passcode: @f7pG*\n \nIf you join by phone only without the Zoom lin k:\n* Dial: +1 669 254 5252 or +1 646 828 7666 or +1 669 216 1590 or +1 55 1 285 1373 or 833 568 8864 (Toll Free) \n* Webinar ID: 161 453 1941\n* Pas scode: 561811\n \n DTEND;TZID="Eastern Standard Time":20220301T140000 DTSTAMP:20220113T224244Z DTSTART;TZID="Eastern Standard Time":20220301T130000 LAST-MODIFIED:20220113T224244Z PRIORITY:5 SEQUENCE:0 SUMMARY;LANGUAGE=en-us:FDA/CDRH Webinar - Principles for Selecting\, Develo ping\, Modifying\, and Adapting Patient-Reported Outcome Instruments for U se In Medical Device Evaluation\, Final Guidance TRANSP:OPAQUE UID:040000008200E00074C5B7101A82E0080000000000F629B3A408D801000000000000000 010000000CF14A679EC363949885A00A398C08EEF X-ALT-DESC;FMTTYPE=text/html:\n\n\n

Date/Time: March 01\, 2022 ( Tuesday)\, from 1 –\; 2 pm ET

& nbsp\;

Background:

The U.S. Food and Drug Administration (FDA)\, Center for Devi ces and Radiological Health (CDRH)\, will host a public webinar about the Final Guidance “\;Principles for Selecting\, Developing\, Modifyin g\, and Adapting Patient-Reported Outcome Instruments for Use In Medical D evice Evaluation.”\;

 \ ;

During this webinar\, the FDA will provide h ighlights of the final guidance and answer questions from webinar attendee s.

 \;

 \;

Webinar Connection Details< o:p>

We encourage you to join at least 15 minutes prior to the start of the webinar. You do not need to register to attend. We recommend you join using the Zoom link below\, if possible:

 \;

 \;

< p class=MsoNormal style='background:white'>I f you join by phone only without the Zoom link:

< ul style='margin-top:0in' type=disc>
  • Dial: +1 669 254 5252 or +1 646 828 7666 or +1 669 216 1590 or +1 551 285 1373 or 833 568 8864 (Toll Free) \;
  • Webinar I D: 161 453 1941
  • Passcode: 561811

    •  \;

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