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DTSTART:19700308T020000
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UID:2140535:Event:78837
DTSTAMP:20260524T221826Z
SUMMARY:FDA Audit Checklist Clinical Trials Seminar 2018
DESCRIPTION:Overview:\nFDA's inspection program follows well-establish
 ed procedures and conducts the inspections with as much consistency as
  possible. FDA trains its investigators from day one. During the first
  six months, they attend extensive classroom and hands on training. FD
 A investigators learn basic skills. As time goes on, special training 
 is given and the field staff use detailed reference materials to guide
  their thinking, actions, decisions and conclusions.\nLocation:  Seat
 tle, WA Date: April 26th & 27th, 2018 and Time: 9:00 AM to 6:00 PM\nV
 enue:  Courtyard Seattle Sea-Tac Area   16038 West Valley Highway T
 ukwila Washington 98188 USA \nPrice:\nRegister now and save $200. (
 Early Bird)\nPrice: $1,295.00 (Seminar Fee for One Delegate)\nUntil Ma
 rch 10, Early Bird Price: $1,295.00 From March 11 to April 24, Regul
 ar Price: $1,495.00\nRegister for 5 attendees   Price: $3,885.00 
      $6,475.00 You Save: $2,590.00 (40%)*\nRegister for 10 att
 endees   Price: $7,122.00   $12,950.00 You Save: $5,828.00 (4
 5%)*\nSponsorship Program benefits for “Quality Assurance Auditing f
 or FDA Regulated Industry” seminar\nAt this seminar, world-renowned 
 FDA Regulated Industry subject matter experts interact with CXO’s of
  various designations. Executives who carry vast experience about FDA 
 Regulated Industry and Experts get down to discussing industry-related
  best practices, regulatory updates, changes in technologies, and much
  more relating to FDA Regulated Industry.\nAs a sponsor of these semin
 ars, you get the opportunity to have your product and company reach ou
 t to C-Level executives in FDA Regulatory -related industries and beco
 me known among these elite executives and subject matter experts. Apar
 t from being seen prominently at these globally held seminars, you als
 o get talked about frequently in our correspondences with our experts 
 and these participants.\nFor More Information- https://www.globalcompl
 iancepanel.com/control/sponsorship \nContact us today!\nNetZealous LL
 C DBA GlobalCompliancePanel\njohn.robinson@globalcompliancepanel.com 
  \nsupport@globalcompliancepanel.com \nToll free: +1-800-447-9407\nP
 hone: +1-510-584-9661\n Website: http://www.globalcompliancepanel.com
 \n \nRegistration Link - https://www.globalcompliancepanel.com/contro
 l/globalseminars/~product_id=901411SEMINAR?SEO\nFollow us on LinkedIn:
  https://www.linkedin.com/company/globalcompliancepanel/\nLike us our 
 Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePan
 el/\nFollow us on Twitter: https://twitter.com/GCPanel\n\nFor more inf
 ormation visit https://medtechiq.ning.com/events/fda-audit-checklist-c
 linical-trials-seminar-2018
DTSTART;TZID=America/New_York:20180426T090000
DTEND;TZID=America/New_York:20180427T180000
CATEGORIES:seminar
LOCATION:Courtyard Seattle Sea-Tac Area
WEBSITE:https://www.globalcompliancepanel.com/control/globalseminars/~
 product_id=901411SEMINAR?april-2018-seo-medtechiq
URL:https://www.globalcompliancepanel.com/control/globalseminars/~prod
 uct_id=901411SEMINAR?april-2018-seo-medtechiq
CONTACT:18004479407
ORGANIZER;CN="John Robinson":https://medtechiq.ning.com/profile/JohnRo
 binson
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562017220?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
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