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TZID:America/New_York
X-LIC-LOCATION:America/New_York
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TZOFFSETFROM:-0500
TZOFFSETTO:-0400
TZNAME:EDT
DTSTART:19700308T020000
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BEGIN:VEVENT
UID:2140535:Event:68968
DTSTAMP:20260518T023455Z
SUMMARY:Webinar on SOPs and Documents
DESCRIPTION:Description :\nThis webinar will explain the basic princip
 les of SOPs and Documentation required for the successful and complian
 t function of a quality system in the pharma and medical device indust
 ries. Particular emphasis will be the specific requirements set out in
  21 CFR Part 210/211/820 and how these requirements can be met.\nYou w
 ill learn the current industry standards for creating and maintaining 
 SOPs and documentation in compliance to GMP requirements.\nAreas Cover
 ed in the Session :\nSOP and documentation requirements\nTraining requ
 irements\nSOP and document archiving\nSOP creation and obsoletion trac
 eability\nInteractive Q&A Session\nWho Will Benefit:\nQuality Control 
 Departments\nQuality Assurance Departments\nProduction Departments\nPu
 rchasing Departments\nOperations Departments\nHR Departments\n\nFor mo
 re information visit https://medtechiq.ning.com/events/webinar-on-sops
 -and-documents
DTSTART;TZID=America/New_York:20160401T130000
DTEND;TZID=America/New_York:20160401T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1724
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1724
CONTACT:4169154458
ORGANIZER:Compliance Trainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
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