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:20220126T181632Z DESCRIPTION:Date/Time: March 22\, 2022 (Tuesday)\, from 1 ā€“ 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 ā€œPatient Engagement in the Design and Conduct of Medical D evice Clinical Studies.ā€\n \nDuring this webinar\, the FDA will provide highlights of the final guidance and answer questions from webinar attende es.\n \n \nWebinar Connection Details\nWe encourage you to join at least 1 5 minutes prior to the start of the webinar. You do not need to register t o attend. We recommend you join using the Zoom link below\, if possible:\n \n* Webinar Link: https://fda.zoomgov.com/j/1613159156?pwd=YkdrNTc1Sk9VOW E4OStFQWZRTHltdz09\n* Passcode: 2NzF+?\n \nIf you join by phone only witho ut the Zoom link:\n* Dial: +1 669 254 5252 or +1 646 828 7666 or +1 669 21 6 1590 or +1 551 285 1373 or 833 568 8864 (Toll Free) \n* Webinar ID: 161 315 9156\n* Passcode: 426760\n \n DTEND;TZID="Eastern Standard Time":20220322T140000 DTSTAMP:20220126T181632Z DTSTART;TZID="Eastern Standard Time":20220322T130000 LAST-MODIFIED:20220126T181632Z PRIORITY:5 SEQUENCE:0 SUMMARY;LANGUAGE=en-us:FDA/CDRH Webinar - Patient Engagement in the Design and Conduct of Medical Device Clinical Studies\, Final Guidance TRANSP:OPAQUE UID:040000008200E00074C5B7101A82E0080000000020F7D60FA208D801000000000000000 0100000009FD1E820DAFCA847A9279921A5D067CB X-ALT-DESC;FMTTYPE=text/html:

Date/Time: March 22\, 2022 (Tuesday)\, from 1 – \; 2 pm ET

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Background:

The U.S. Fo od and Drug Administration (FDA)\, Center for Devices and Radiological Hea lth (CDRH)\, will host a public webinar about the Final Guidance “\;< b>Patient Engagement in the Design and Conduct of Medical Device Clinical Studies.”\;

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During this webinar\, the FDA will provide highlights of the final guidance and answer questions from webinar attendees.

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Webinar Connection Details

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

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If you join by phone only without the Zoom link:

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