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METHOD:PUBLISH
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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
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DTSTART:19701101T020000
RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU
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BEGIN:VEVENT
UID:2140535:Event:63982
DTSTAMP:20260518T085251Z
SUMMARY:Webinar On Project Management for Computer Systems Validation
DESCRIPTION:Project Management is defined as the planning and organiza
 tion of an organization's resources in order to move a specific task, 
 event or duty toward completion. However, Validation of Computerized S
 ystems has a very specific set of tasks that are often mismanaged, res
 ulting in missed deadlines, increased costs, and regulatory risk, and 
 missed times to market for a company’s product. Per the CDRH, 20% of
  product recalls in the medical device industry are due to faulty soft
 ware!!! Yet, these human, financial and reputation capital expensive i
 ssues, can be averted with computerized systems validation and 21 CFR 
 11 compliance.\nThe Project Manager for a Validated Computerized Syste
 m, has to deliver on time and on budget, but with the added risk of ha
 ving to meet regulatory compliance, often causing project overruns, re
 gulatory findings and missed times to market.\nThis detailed webinar w
 ill explain the basic tenets of project management, the basic tenets o
 f 21 CFR 11 compliance for Computer Systems Validation and will show h
 ow to marry the two, to deliver on time and on budget while meeting re
 gulatory compliance requirements in a more effective manner.\nAreas Co
 vered in the Session :\nBasics of Project Management\n21 CFR 11 and Co
 mputer Systems Validation (CSV)\nProject Planning for a Computer Syste
 ms Validation Project\nCSV Deliverables\nHiddent CSV Deliverables\nMet
 rics & Gantt Charts\nCommon Pitfalls and How to Avoid them\nThe 10 Dea
 dly Sins!!\nWho Will Benefit:\nProject Managers\nIT Management\nBusine
 ss Process Owners\nQuality Managers\nQuality Engineers\nGxP\nConsultan
 ts\nPrice Tags:\nLive\nSingle Live : For One Participant\n$ 249\nCorpo
 rate Live : For Max. 10 Participants\n$ 899\nRecording\nSingle REC : F
 or One Participant - Unlimited Access for 6 Months\n$ 299\n\nFor more 
 information visit https://medtechiq.ning.com/events/webinar-on-project
 -management-for-computer-systems-validation
DTSTART;TZID=America/New_York:20140808T130000
DTEND;TZID=America/New_York:20140808T150000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=IT1058
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=IT1058
CONTACT:4169154458
ORGANIZER;CN=compliancetrainings:https://medtechiq.ning.com/profile/co
 mpliancetrainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
END:VEVENT
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