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X-WR-CALDESC:Events for Novatek International
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DTSTART:20250101T000000
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DTSTART;TZID=Asia/Singapore:20260526T100000
DTEND;TZID=Asia/Singapore:20260526T120000
DTSTAMP:20260524T224758
CREATED:20260422T185614Z
LAST-MODIFIED:20260504T192603Z
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SUMMARY:Webinar - Stability Data Evaluation and Trend Analysis per ICH Q1E
DESCRIPTION:Stability Data Evaluation and Trend Analysis per ICH Q1E: Principles and Best Practices \nWebinar \n26 May 2026| Tuesday| 10:00AM\, SGT \nRegistration Link: https://tinyurl.com/NovatekSTB \nVivien Santillan – Novatek International \nKim HuynhBa – PHARMALYTIK \n  \nIn an era where product quality\, regulatory alignment\, and data-driven decision‑making define competitive advantage\, the ability to evaluate stability data with scientific rigor has never been more essential. ICH Q1E remains a cornerstone guideline for establishing\, justifying\, and defending shelf-life decisions—yet its practical application continues to challenge many organizations\, especially as data volumes grow and digital transformation accelerates. \n  \nJoin us for a focused and highly practical webinar designed to strengthen your understanding of stability data evaluation and trend analysis in accordance with ICH Q1E. This session brings together deep regulatory insight\, scientific grounding\, and modern digital approaches to help you elevate your stability program and lifecycle management strategies. \n#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/webinar-stability-data-evaluation-and-trend-analysis-per-ich-q1e/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/NTINT-Webinar-Stability-2026-May.png
ORGANIZER;CN="Novatek International":MAILTO:webinars@ntint.com
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20260602
DTEND;VALUE=DATE:20260604
DTSTAMP:20260524T224758
CREATED:20260427T161030Z
LAST-MODIFIED:20260504T192455Z
UID:20440-1780358400-1780531199@ntint.com
SUMMARY:KENX - COMPUTER SYSTEMS\, SOFTWARE & AI VALIDATION UNIVERSITY EUROPE
DESCRIPTION:Look for Susan Cleary‘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/
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ORGANIZER;CN="KENX":MAILTO:info@kenx.org
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20260602
DTEND;VALUE=DATE:20260605
DTSTAMP:20260524T224758
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
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20260609
DTEND;VALUE=DATE:20260611
DTSTAMP:20260524T224758
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/
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ORGANIZER;CN="Systec & Solutions":MAILTO:talk@systec-solutions.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260611
DTEND;VALUE=DATE:20260612
DTSTAMP:20260524T224758
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
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