BEGIN:VCALENDAR
PRODID:NingEventWidget-v1
VERSION:2.0
METHOD:PUBLISH
BEGIN:VTIMEZONE
TZID:America/New_York
X-LIC-LOCATION:America/New_York
BEGIN:DAYLIGHT
TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:19700308T020000
RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:-0400
TZOFFSETTO:-0500
TZNAME:EST
DTSTART:19701101T020000
RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
UID:2140535:Event:72127
DTSTAMP:20260507T044701Z
SUMMARY:Applied Statistics for FDA Process Validation 2017
DESCRIPTION: \nCourse \"Applied Statistics for FDA Process Validation
 \" has been pre-approved by RAPS as eligible for up to 12 credits 
 towards a participant's RAC recertification upon full completion.\nOve
 rview:\nIn Guidance for Industry Process Validation: General Principle
  and Practices, process validation is defined as, \"\"...the collectio
 n and evaluation of data, from the process design stage through commer
 cial production..\" The guidance further delineates the 'process desig
 n stage through commercial production' into three distinct stages of t
 he product lifecycle:\nStage 1: Process Design: The commercial manufa
 cturing process is defined during this stage based on knowledge gained
  through development and scale-up activities.\nStage 2: Process Quali
 fication: During this stage, the process design is evaluated to determ
 ine if the process is capable of reproducible commercial manufacturing
 .\nStage 3: Continued Process Verification: Ongoing assurance is gain
 ed during routine production that the process remains in a state of co
 ntrol.\nThe first stage of process validation is process design. The P
 rocess Validation guidance document states, \"A successful validation 
 program depends on information and knowledge from product and process 
 development. This knowledge and understanding is the basis for establi
 shing an approach to control of a manufacturing process that results i
 n products with desired quality attributes:\n\n \nLocation: San Dieg
 o, CA Date: April 20th & 21st, 2017 and Time: 9:00 AM to 6:00 PM\n \n
 Venue: Four Points by Sheraton San Diego Downtown\nAddress:  1617 1st
  Avenue - San Diego, California, 92101 - United States\n \nPrice:\n 
 \nRegister now and save $200. (Early Bird)\n \nPrice: $1,295.00 (Semi
 nar Fee for One Delegate)\n \nUntil March 15, Early Bird Price: $1,29
 5.00 From March 16 to April 18, Regular Price: $1,495.00\n \nRegister
  for 5 attendees   Price: $3,885.00 $6,475.00 You Save: $2,590.00 (4
 0%)*\n \n \nQuick Contact:\nNetZealous DBA as GlobalCompliancePanel\
 n \nPhone: 1-800-447-9407\nFax: 302-288-6884\nEmail: support@globalco
 mpliancepanel.com               \n\nFollow us on LinkedI
 n: https://www.linkedin.com/company/globalcompliancepanel?\nLike us ou
 r Facebook page: https://www.facebook.com/TrainingsAtGlobalComplianceP
 anel/\nFollow us on Twitter: https://twitter.com/GCPanel\n \n \n \n
 \n\n\nFor more information visit https://medtechiq.ning.com/events/app
 lied-statistics-for-fda-process-validation-2017
DTSTART;TZID=America/New_York:20170420T090000
DTEND;TZID=America/New_York:20170421T180000
CATEGORIES:applied, statistics, for, fda, process, validation, 2017
LOCATION:San Diego, CA
WEBSITE:http://www.globalcompliancepanel.com/control/globalseminars/~p
 roduct_id=900806SEMINAR?channel=mailer&camp=Seminar&AdGroup=medtechiq_
 April_2017_SEO
URL:http://www.globalcompliancepanel.com/control/globalseminars/~produ
 ct_id=900806SEMINAR?channel=mailer&camp=Seminar&AdGroup=medtechiq_Apri
 l_2017_SEO
CONTACT:800-447-9407
ORGANIZER:NetZealous DBA as GlobalCompliancePanel
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562014967?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob
 inson":https://medtechiq.ning.com/profile/JohnRobinson
END:VEVENT
END:VCALENDAR