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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
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BEGIN:VEVENT
UID:2140535:Event:69850
DTSTAMP:20260517T215226Z
SUMMARY:Webinar On Basic Requirements for IQ, OQ and PQ Quality Protoc
 ols
DESCRIPTION:Description:\nCurrent regulatory requirements state the ne
 ed to prove equipment, systems and utilities are verified to perform t
 heir desired functions. This verification comes in the form of qualifi
 cation protocols that verify proper installation, operation over its e
 ntire range, and acceptable performance according to established proce
 dures and operational set points. This webinar will provide an outline
  of the typical documents used for qualification activities, the type 
 of information normally included in each and the common deficiencies c
 ited when audited. Attendees will be given the chance to ask questions
  regarding their own protocols and actual case studies will be used to
  highlight various points.\nThis webinar will highlight the importance
  of establishing specifications, proper documentation with regards to 
 results obtained, how to address deviations encountered and how best t
 o summarize results obtained.\nAny equipment, system or utility used f
 or GMP impacted products or services must demonstrate they are suitabl
 e for their intended use and operate according to their design. To pro
 ve these requirements, the protocols developed for both installation a
 nd operational verification (and others) are expected to be in place a
 nd approved prior to use. This webinar, designed for those just starti
 ng to be responsible for qualification activities, will help establish
  an outline of the basic components for these two protocols. In additi
 on, common deficiencies cited by regulators will also be reviewed in o
 rder to help attendees avoid similar issues when their protocols are a
 udited.\nAreas Covered in the Session :\nReview common protocol types 
 and the typical information included in each.\nDiscuss common deficien
 cies cited with each type.\nReview how best to summarize results and t
 he handling of deviations encountered\nDiscuss questions that attendee
 s may have regarding their current practices.\nWho Will Benefit:\nQual
 ity Assurance Teams\nQuality Control Teams\nManufacturing Teams\nProdu
 ction Teams\nRegulatory Teams\nLaboratory Personnel\nManagement Teams\
 n\nFor more information visit https://medtechiq.ning.com/events/webina
 r-on-basic-requirements-for-iq-oq-and-pq-quality-protocol-1
DTSTART;TZID=America/New_York:20160711T130000
DTEND;TZID=America/New_York:20160711T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1668
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1668
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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