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DTSTART:19700308T020000
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UID:2140535:Event:62127
DTSTAMP:20260522T171150Z
SUMMARY:Process Validation for Medical Devices
DESCRIPTION:Medical device manufacturers can avoid FDA Warning Letters
 , 483s and enforcement actions with a good understanding process valid
 ation principles. But knowing how to proceed is the toughest task as n
 o FDA guidance document is available which talks about it.\nThis two d
 ay interactive seminar is designed to make you understand the regulato
 ry requirements of both FDA QSR and ISO 13485:2003. To compensate for 
 the missing guidance document, the course draws the “how to” answe
 r from various other sources including the GHTF guidance, FDA’s QSIT
 , FDA Warning Letters, and the guidance document for ISO 13485:2003. T
 his course will help attendees understand the regulatory requirements 
 and the statistical methods needed to perform effective process valida
 tion for medical device manufacturing.\nFor Registration:\nhttp://www.
 complianceonline.com/ecommerce/control/seminar?product_id=80108SEM&?ch
 annel=meditechiq\n\nFor more information visit https://medtechiq.ning.
 com/events/process-validation-for-medical-devices
DTSTART;TZID=America/New_York:20130821T080000
DTEND;TZID=America/New_York:20130822T170000
CATEGORIES:seminar
LOCATION:Courtyard Marriott Boston   ,MA 02139, USA
WEBSITE:
URL:
CONTACT:+1-650-620-3915
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562006570?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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