BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20200122T130000 DTEND:20200122T143000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT UID:20200122T000000-2027226293-example.com DTSTAMP:20200122T000000 DTSTART;TZID="US/Eastern":20200122T130000 DTEND;TZID="US/Eastern":20200122T143000 SUMMARY:Ensuring Your Site is Ready for an FDA Inspection DESCRIPTION: Although an effective Quality Management System should always be inspection ready, many medical device companies make basic mistakes during FDA inspections leading to 483s and even warning letters.  This webinar will help you create an inspection readiness plan, so you are well prepared for an FDA inspection. PRIORITY:3END:VEVENT END:VCALENDAR