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:470994
DTSTAMP:20260409T182601Z
SUMMARY:Human Errors in GMP Manufacturing and Laboratory Processes Ide
 ntification
DESCRIPTION:This instructor-led live training webinar will discuss reg
 ulatory requirements for detecting, correcting and preventing human er
 rors in manufacturing and laboratory environments as well as developin
 g a competent, effective corrective and preventive action system.\nWhy
  Should You Attend:\nAnalysis of investigation reports reveal that hum
 an error is one of the top root causes for deviations, discrepancies a
 nd quality incidents in pharmaceutical manufacturing. And when you exa
 mine the CAPA's that are developed from these, retraining and rewrite 
 of SOP is top the list. Yet on further re-examination, you find that t
 hese problems keep resurfacing again and again. Put in another way, th
 e CAPA's are ineffective. Does it mean that the CAPA's were wrong or i
 s it pointing to another problem? Namely, that the investigation did n
 ot pinpoint the root cause of or most probable contributing factors to
  the problem. Most often \"human error\" is not really the problem but
  a symptom of a system or facility or operation that is not designed t
 o be run by humans. Humans do contribute to problems but more often th
 an not, because what we are asking them to do is not designed with hum
 ans in mind. So a true CAPA should be developed to solve the problems 
 with the system, facility and operation rather than focus on remediati
 on of people. This requires investigations to focus on getting to the 
 real root cause and contributing factors.\n\nAreas Covered in the Webi
 nar:\n\nIdentify why human error is often designated the root cause of
  deviations and discrepancies.\nIdentify why your CAPA's are less effe
 ctive than you hoped.\nUnderstand why human error is not the real caus
 e of the deficiencies and deviations.\nHow to probe further to identif
 y the causes or contributing factors that really cause the problems yo
 u are seeing.\nHow to develop a true CAPA for these problems.\nDevelop
  an efficient and effective CAPA system to remedy the ingrained proble
 ms.\nIdentification and prevention of human error during data entry.\n
 \nWho Will Benefit:\n\nQuality Assurance Personnel\nQuality Control Pe
 rsonnel\nSupply Chain and Logistics Managers\nRegulatory Affairs Profe
 ssionals\nProcess Development Scientists and Management\nManufacturing
  Management and Scientists\nProject Managers working in the CMC arena\
 n\n\nFor more information visit https://medtechiq.ning.com/events/huma
 n-errors-in-gmp-manufacturing-and-laboratory-processes
DTSTART;TZID=America/New_York:20220224T100000
DTEND;TZID=America/New_York:20220224T130000
CATEGORIES:webinar
LOCATION:online
WEBSITE:https://www.complianceonline.com/human-errors-gmp-manufacturin
 g-laboratory-processes-webinar-training-706786-prdw?channel=MedTech%20
 I.Q
URL:https://www.complianceonline.com/human-errors-gmp-manufacturing-la
 boratory-processes-webinar-training-706786-prdw?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/10061242458?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
END:VEVENT
END:VCALENDAR