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BEGIN:VEVENT
UID:20261012T011339Z - 62997@eupp224
DTSTART;TZID=Africa/Cairo:20261211T153000
DTEND;TZID=Africa/Cairo:20270115T190000
CREATED:20261012T011339Z
DESCRIPTION:<a href="https://www.valoregypt.com/event/advanced-computerized
 -systems-validation-workshop-csv-b26-139/register">Advanced Computerized S
 ystems Validation Workshop ( CSV) b26</a>\nThe Advanced Computerized Syste
 ms Validation (CSV) Workshop provides a deep and practical understanding o
 f how to validate computerized systems used in GMP-regulated environments.
  Participants will explore the complete lifecycle approach to CSV — from
  planning and risk assessment to execution\, documentation\, and maintaini
 ng a validated state. This workshop bridges regulatory expectations such a
 s EU Annex 11\, FDA 21 CFR Part 11\, and GAMP 5\, emphasizing data integri
 ty\, system security\, and audit readiness. Through real-life examples\, t
 emplates\, and validation case studies\, participants will learn to implem
 ent effective\, compliant\, and sustainable validation programs for labora
 tory\, production\, utilities\, and quality systems. For More -->
DTSTAMP:20261012T011339Z
LOCATION:VOLAR PRO\, 22 عمارات العبور\, Salah Salem S\, الق
 اهرة Cairo\, 11725\, Egypt
SUMMARY:Advanced Computerized Systems Validation Workshop ( CSV) b26
X-ALT-DESC;FMTTYPE=text/html:<a href="https://www.valoregypt.com/event/adva
 nced-computerized-systems-validation-workshop-csv-b26-139/register">Advanc
 ed Computerized Systems Validation Workshop ( CSV) b26</a>\nThe Advanced C
 omputerized Systems Validation (CSV) Workshop provides a deep and practica
 l understanding of how to validate computerized systems used in GMP-regula
 ted environments. Participants will explore the complete lifecycle approac
 h to CSV — from planning and risk assessment to execution\, documentatio
 n\, and maintaining a validated state. This workshop bridges regulatory ex
 pectations such as EU Annex 11\, FDA 21 CFR Part 11\, and GAMP 5\, emphasi
 zing data integrity\, system security\, and audit readiness. Through real-
 life examples\, templates\, and validation case studies\, participants wil
 l learn to implement effective\, compliant\, and sustainable validation pr
 ograms for laboratory\, production\, utilities\, and quality systems. For 
 More -->
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