BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Novatek International - ECPv6.16.3//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://ntint.com
X-WR-CALDESC:Events for Novatek International
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:UTC
BEGIN:STANDARD
TZOFFSETFROM:+0000
TZOFFSETTO:+0000
TZNAME:UTC
DTSTART:20250101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260602
DTEND;VALUE=DATE:20260604
DTSTAMP:20260601T175344
CREATED:20260427T161030Z
LAST-MODIFIED:20260529T174201Z
UID:20440-1780358400-1780531199@ntint.com
SUMMARY:KENX - COMPUTER SYSTEMS\, SOFTWARE & AI VALIDATION UNIVERSITY EUROPE
DESCRIPTION:Look for Niccolo Moreno‘s talk & don’t forget to connect with Angel Ruiz for more risk management information.\n\nREGISTER: CVS/CSA University Europe 2026\n  \nCSV & CSA University brings together experts across validation\, quality\, IT\, and digital systems for two days of practical\, implementation-focused training. The program emphasizes modern\, risk-based approaches aligned with global expectations\, including EU Annex 11\, the emerging Annex 22 draft\, and contemporary CSA principles for streamlining computerized system assurance. As organizations manage a mix of legacy platforms\, cloud solutions\, and AI-enabled technologies\, attendees will gain real-world strategies\, templates\, and examples to strengthen compliance while modernizing validation practices across today’s evolving GxP landscape. \n\nWhat You’ll Learn\n\n\n\nHow to operate CSA while maintaining compliance across validation\, quality\, and IT\nModern risk-based approaches that reduce documentation burden and accelerate system readiness\nBest practices for vendor audits\, upgrades\, SaaS/Cloud validation\, mobile apps\, automation\, and digital systems\nWhere emerging digital and AI capabilities fit into CSV/CSA frameworks\, including governance\, guardrails\, and human-in-the-loop
URL:https://ntint.com/event/kenx-computer-systems-software-ai-validation-university-europe/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/23.-KENX-CSVCSA-Ireland.png
ORGANIZER;CN="KENX":MAILTO:info@kenx.org
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260602
DTEND;VALUE=DATE:20260605
DTSTAMP:20260601T175344
CREATED:20260430T183020Z
LAST-MODIFIED:20260504T192703Z
UID:20444-1780358400-1780617599@ntint.com
SUMMARY:CHPI Americas
DESCRIPTION:Find Nicholas Gavrielides and Gregory Froundjian at this year’s CPHI Americas in Philadelphia on June 2-4\, 2026.\nCompliance pressure is tightening across every layer of pharmaceutical manufacturing—yet validation timelines\, fragmented systems\, and data integrity risks continue to slow down release cycles and increase audit exposure. \nNovatek International will be attending CPHI Americas with on-site representation from Nicholas Gavrielides and Gregory Froundjian\, engaging with industry leaders driving the next wave of digital transformation in regulated environments. \n📍 Event: CPHI Americas \n📅 Date: June 2–4\, 2026 \n📍 Location: Pennsylvania Convention Center\, Philadelphia\, USA \nThis year’s event focuses on contract manufacturing innovation\, the shift from CSV to CSA\, AI-enabled validation\, and end-to-end digitalization of pharma operations—directly addressing today’s biggest challenges in compliance burden\, siloed data\, and manufacturing risk. \nNovatek International supports organizations with integrated digital solutions that enable paperless validation\, strengthen audit readiness\, improve data integrity\, and streamline QC\, manufacturing\, and quality workflows across the full GxP lifecycle. \nRegister Here: https://www.cphi.com/americas/\nExplore Novatek’s event page: https://ntint.com/event/chpi-americas/ \nVisit https://ntint.com/ to see how digital validation and quality systems can reduce compliance risk and accelerate manufacturing efficiency across regulated environments. \nWhere do you see the biggest bottleneck today—validation workload\, or data integrity across systems? \n#PharmaManufacturing #QualityAssurance #CSV #GxP #DigitalTransformation #Digitalization #Digitization #PharmaCompliance #RegulatoryCompliance #QualityManufacturing #DigitalTransformation #PharmaQuality #DrugManufacturing #GMPCompliance #RegulatoryTech #ContaminationControl #QualityManagement #ProcessAutomation #PharmaTechSolutions #ComplianceSoftware #LIMSolutions #PharmaRegulatory #BiotechSoftware #PharmaDigitalization #DataDrivenDecisions #RegulatorySolutions #LifeScienceTech #ManufacturingSolutions #ProductSafety #EUAnnex1 #InnovationInPharma #ComplianceManagement #RegulatoryStandards #PharmaInnovation #QualityAssurance #ComplianceIntegration #PharmaDataManagement #RegulatoryRequirements #DigitalCompliance #PharmaAutomation #ComplianceUpdates #RegulatoryAdherence
URL:https://ntint.com/event/chpi-americas/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/22.-CPHI-Americas.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260609
DTEND;VALUE=DATE:20260611
DTSTAMP:20260601T175344
CREATED:20260506T182652Z
LAST-MODIFIED:20260506T182652Z
UID:20464-1780963200-1781135999@ntint.com
SUMMARY:Systec & Solutions - Life Science Ready Days
DESCRIPTION:Don’t miss Susan Cleary (Novatek International) and John Brett‘s (Sanofi) collaborative talk at the 2026 Life Science Ready Days event by Systec & Solutions.\n“Modernizing Clear Room Sample Collection and Reporting”\nRegister Here: Life Science Ready Days 2026\n  \nEvent Details: \nDATE: June 9-10\, 2026 \nLocation: Karlsruhe\, Germany \n  \nPresentation Key Points\n\nLearn how digital sample collection workflows can improve compliance in clean room operations.\nUnderstand how autosave\, direct data entry\, and electronic records strengthen data integrity and reduce data loss risk.\nSee how guided workflows and automated traceability reduce manual errors and improve record reliability.\nLearn how moving from paper-based processes to digital sample collection can improve efficiency and support a paperless lab.\nGain practical insight from a real facility case study\, including lessons learned from an FDA audit focused on environmental monitoring and contamination control.\n\n  \nWhy you should attend\n\nInspiring content\nDiscover cutting-edge topics\, technologies\, and trends from across the pharma and life science landscape ‒ delivered by leading keynote speakers and hands-on experts.\nInteractive workshops\nTake part in collaborative sessions that are tailored to the real-world challenges of modern pharmaceutical operations and regulatory frameworks.\nGenuine networking\nMeet and connect with peers\, innovators\, and key players from your field ‒ whether during the sessions\, over coffee\, or as part of the evening events.
URL:https://ntint.com/event/systec-solutions-life-science-ready-days/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/05/27.-Systec-Solutions-Life-Science-Ready-Days-2026.png
ORGANIZER;CN="Systec & Solutions":MAILTO:talk@systec-solutions.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260610
DTEND;VALUE=DATE:20260612
DTSTAMP:20260601T175344
CREATED:20260529T180001Z
LAST-MODIFIED:20260529T180511Z
UID:20522-1781049600-1781222399@ntint.com
SUMMARY:World Orphan Drug Congress
DESCRIPTION:As regulatory expectations evolve and rare disease therapies become more complex\, life sciences organizations are under increasing pressure to accelerate innovation while maintaining compliance\, quality\, and data integrity. \nREGISTER HERE: https://www.terrapinn.com/conference/world-orphan-drug-congress-usa/index.stm \n  \nThat’s why Novatek International is excited to announce that Vicky Azadian will be attending the World Orphan Drug Congress USA 2026\, taking place June 9–11\, 2026 at the Thomas M. Menino Convention & Exhibition Center in Boston\, MA. The event brings together global leaders across pharma\, biotech\, regulatory agencies\, patient advocacy groups\, and technology providers focused on advancing rare disease and orphan drug development. \n  \nKey discussions will explore AI\, digital health\, regulatory strategy\, advanced therapies manufacturing\, patient data\, and scalable clinical and manufacturing operations — all critical areas for organizations navigating increasing compliance demands and operational risk. \n  \nNovatek International helps pharmaceutical manufacturers modernize validation\, strengthen audit readiness\, improve data integrity\, and streamline GxP workflows through connected digital quality and manufacturing solutions. \n  \n🔹 Learn more or register for the event: World Orphan Drug Congress USA 2026\n🔹 Visit Novatek International to discover how digital transformation can reduce validation effort\, improve compliance readiness\, and support more efficient pharmaceutical manufacturing operations. \n  \n#PharmaManufacturing #RareDisease #GxP #QualityAssurance #DigitalTransformation \n  \nWhat do you see as the biggest operational challenge facing rare disease and orphan drug manufacturers today?
URL:https://ntint.com/event/world-orphan-drug-congress/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/05/28.-World-Orphan-Drug-Congress-1.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260611
DTEND;VALUE=DATE:20260612
DTSTAMP:20260601T175344
CREATED:20260520T152813Z
LAST-MODIFIED:20260521T163014Z
UID:20512-1781136000-1781222399@ntint.com
SUMMARY:PDA Canada
DESCRIPTION:Come meet Bob Hady and Jadzia Famili at the PDA Canada Networking event in Mississauga\, Ontario!\nPDA Canada Chapter: Networking Event | PDA \n 
URL:https://ntint.com/event/pda-canada/
CATEGORIES:Workshop
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/05/29-PDA-Canada.png
END:VEVENT
END:VCALENDAR