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DTSTART;VALUE=DATE:20260602
DTEND;VALUE=DATE:20260605
DTSTAMP:20260606T050131
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:20260602
DTEND;VALUE=DATE:20260604
DTSTAMP:20260606T050131
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;TZID=Asia/Singapore:20260526T100000
DTEND;TZID=Asia/Singapore:20260526T120000
DTSTAMP:20260606T050131
CREATED:20260422T185614Z
LAST-MODIFIED:20260504T192603Z
UID:20434-1779789600-1779796800@ntint.com
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
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260517
DTEND;VALUE=DATE:20260518
DTSTAMP:20260606T050131
CREATED:20260420T144046Z
LAST-MODIFIED:20260427T154523Z
UID:20430-1778976000-1779062399@ntint.com
SUMMARY:StabilityHub - Pharmaceutical Stability Discussion Group (PSDG)
DESCRIPTION:We’re thrilled to announce that Corinne Cleary\, will be speaking at the upcoming StabilityHub: Pharmaceutical Stability Discussion Group (PSDG) In‑Person Meeting – Spring 2026\, taking place May 17–19 in Wilson\, NC (Raleigh/Durham area)! \nThis premier event brings together stabilitarians\, industry stakeholders\, and service providers for presentations\, Q&A sessions\, benchmarking discussions\, best practices exchanges\, vendor exhibits\, and a facility tour focused on advancing knowledge in pharmaceutical stability and manufacturing. \nWe’re also excited that Gregory Froundjian will be attending — ready to help you reduce risk in your pharmaceutical manufacturing process and share insights on improving stability practices. \n👉 Register for the PSDG Spring 2026 meeting and secure your spot: https://lnkd.in/eA-ZVvb7 \nWhether you’re looking to connect with peers\, gain practical knowledge\, or elevate your stability strategies\, this event is a must‑attend for industry professionals.
URL:https://ntint.com/event/stabilityhub-pharmaceutical-stability-discussion-group-psdg/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/18.-StabilityHub-PSDG.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260514
DTEND;VALUE=DATE:20260515
DTSTAMP:20260606T050131
CREATED:20260417T151353Z
LAST-MODIFIED:20260417T151353Z
UID:20428-1778716800-1778803199@ntint.com
SUMMARY:PDA Metro - Chapter Day
DESCRIPTION:Looking forward to Susan Cleary‘s talk at the PDA Metro Chapter – Chapter day event on May 14\, in Ridgefield New Jersey.\n  \nDon’t forget to also introduce yourself to Nicholas Gavrielides from our team to learn more about how to start reducing risk in your process.\n  \nRegister Here\n  \nKey highlights of the agenda include: \n\nContamination Control and Annex 1 with a focus on trending and pattern recognition\nData Integrity 2026\, exploring upcoming expectations and practical readiness strategies\nArtificial Intelligence Applications in streamlining SOP development and improving operational efficiency\nDrug Repurposing Approaches\, from advanced algorithms to regulatory approvals\nAuditing of Pharmaceutical Microbiology Laboratories and strengthening quality systems\nCDMO Capabilities for Advanced Therapies\, including gene and cell therapies\nRisk-Based Packaging Qualification in CDMOs\nGlobal Aseptic Processing Compliance Trends: Enforcement data insights across FDA\, EMA\, and PIC/S agencies.\nContainer Closure Integrity Testing (CCIT) strategies aligned with global regulatory frameworks\n\n  \nRegister Here
URL:https://ntint.com/event/pda-metro-chapter-day/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/19.-PDA-Metro-Chapter-Day.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260512
DTEND;VALUE=DATE:20260514
DTSTAMP:20260606T050131
CREATED:20260417T144217Z
LAST-MODIFIED:20260417T150759Z
UID:20422-1778544000-1778716799@ntint.com
SUMMARY:PDA APAC - Pharmaceutical Manufacturing & Quality Conference 2026
DESCRIPTION:Come meet Neeraj Choudhary \, Regional Director at Novatek International\, at the PDA APAC Pharmaceutical Manufacturing & Quality Conference 2026 in Singapore!\n  \nRegister Here
URL:https://ntint.com/event/pda-apac-pharmaceutical-manufacturing-quality-conference-2026/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/17.-PDA-APAC-Singapore.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260430
DTEND;VALUE=DATE:20260501
DTSTAMP:20260606T050131
CREATED:20260408T155327Z
LAST-MODIFIED:20260408T155356Z
UID:20410-1777507200-1777593599@ntint.com
SUMMARY:PDA Southern California Chapter - Women in Life Sciences
DESCRIPTION:Connect with Cheryl Zamand-Zadeh at the PDA Southern California Chapter: Women in Life Sciences\n  \nRegister Here: PDA Southern California Chapter | PDA
URL:https://ntint.com/event/20410/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/16.-PDA-SoCal-Devices-and-Women-in-Life-Sciences-2.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260421
DTEND;VALUE=DATE:20260424
DTSTAMP:20260606T050131
CREATED:20260408T154758Z
LAST-MODIFIED:20260417T143843Z
UID:20405-1776729600-1776988799@ntint.com
SUMMARY:Interphex 2026
DESCRIPTION:Connect with Nicholas Gavrielides and Sarah Alimirzaei at the Interphex 2026 show in New York.\n  \nRegister Here: https://www.interphex.com/en-us/pricing-page.html \n  \nINTERPHEX\, the leading global pharmaceutical and biotechnology event that fuses industry innovation with expert-led conference. Taking place at the Javits Center NYC on April 21-23\, 2026\, INTERPHEX offers an expansive exhibition floor showcasing cutting-edge products and services from industry leaders. Attendees and exhibitors engage in enlightening seminars led by experts\, delve into technology showcases spotlighting the latest innovations\, and benefit from unparalleled networking opportunities. This dynamic platform unites professionals\, fostering collaborations and providing a comprehensive view of advancements in pharmaceutical manufacturing\, process development\, and regulatory compliance. Elevate your industry knowledge\, connect with key stakeholders\, and stay at the forefront of pharmaceutical innovation at INTERPHEX.
URL:https://ntint.com/event/interphex-2026/
LOCATION:Javits Center\, NYC\, 429 11th avenue\, New York\, NY\, 10001\, United States
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/15.-Interphex.png
ORGANIZER;CN="Interphex":MAILTO:inquiry@interphex.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260420
DTEND;VALUE=DATE:20260423
DTSTAMP:20260606T050131
CREATED:20260224T191335Z
LAST-MODIFIED:20260224T191346Z
UID:20372-1776643200-1776902399@ntint.com
SUMMARY:ISPE Europe Annual
DESCRIPTION:Novatek International will be attending the 2026 ISPE Europe Annual Conference in Copenhagen\, Denmark (20–22 April 2026) — a landmark event for pharmaceutical and biopharmaceutical professionals across the industry.\n  \nBe sure to meet with Agnes Barti on-site to learn more about how to start reducing risk in your process.\n  \nThis year’s conference brings together experts\, innovators\, and leaders to explore how transformative technologies like AI/ML\, virtual and augmented reality\, and smart manufacturing are reshaping our sector.\n  \nRegister here: 2026 ISPE Europe Annual Conference – Copenhagen Denmark | ISPE | International Society for Pharmaceutical Engineering\n  \nHere are a few highlights I’m looking forward to:\nEmerging trends in digital transformation and Pharma 4.0‑enabled manufacturing.\nExpert‑led sessions and case studies focused on operational efficiency\, project success strategies\, and real‑world examples.\nEngaging interactive forums and panel discussions on quality risk management\, open data frameworks\, and regulatory evolution\nOpportunities for networking\, learning\, and professional collaboration with industry stakeholders from around the world.\n  \nWhether discussing sustainability in manufacturing\, digital compliance\, or advanced therapy innovations\, this conference offers a unique platform to exchange insights and help shape the future of pharma engineering.\n  \nLooking forward to connecting with fellow professionals and bringing back fresh perspectives to drive meaningful impact.
URL:https://ntint.com/event/ispe-annual-europe/
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/14.-ISPE-Europe-Annual-Conference.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260413
DTEND;VALUE=DATE:20260418
DTSTAMP:20260606T050131
CREATED:20260408T153821Z
LAST-MODIFIED:20260408T153948Z
UID:20396-1776038400-1776470399@ntint.com
SUMMARY:PDA Brazil - Microbiology Week & Annex 1
DESCRIPTION:Make sure to attend Parsa Famili‘s talk at the PDA Brazil: Microbiology Week & Annex 1 event in Rio de Janeiro and Sao Paulo\, Brazil.\n\nConnect with Stephen Smith for more information on how to reduce risk in your manufacturing process.\n  \nRegister Here: https://pdabrazil.org/eventos/semana-da-microbiologia-e-anexo-i-monitoramento-ambiental-metodos-rapidos-e-investigacao-desvios-2026/#inscricao \n  \nThe main topics covered: \n\nHow to perform Environmental Monitoring – Cleanroom\, Personal Sampling\, Surfaces\, Water\, Sterility Tests\, HEPAs. Viable and non-viable air sampling\nCCS Contamination Control\nUtilities and Facilities (Water\, Gases\, HVAC\, Maintenance and Design)\nMaterial considerations (storage\, handling and transfer to cleanroom)\nStaffing Considerations and Training for Microbiologists (Clothing\, Hygiene\, Flow\, Training\, Qualification\, and Processes)\nSmoke Testing\nManufacturing process considerations (cleaning\, sanitization\, filtration\, and processes)\nBarrier Systems (Isolators\, Gloves and Rabs)\nRapid Methods and Quality Control\nAseptic Processing Simulation – Media Fill\nMicrobial identification and research\nAnalysis of Audit and Inspection Results\nRecovery from downtime and contingency planning\nHPLC Endotoxin Detection/Qualification\nCleaning\, Disinfection\, Decontamination\, Sanitization and Disinfectants.\nClassification of Environmental Isolates\nMeasurement and monitoring of differential pressure in clean areas\nCulture Media and Environmental Monitoring: Interactions\, Performance\, and Compliance with PIC/S Annex 1\nPaving the Way for AI: Risk-Based Cleanliness Validation and Environmental Monitoring through Digitalization – From Reactive to Predictive Control
URL:https://ntint.com/event/pda-brazil-microbiology-week-annex-1/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/04/12.-PDA-Brazil.png
ORGANIZER;CN="PDA Brazil":MAILTO:https://pdabrazil.org/contato/
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260409
DTEND;VALUE=DATE:20260411
DTSTAMP:20260606T050131
CREATED:20260224T213953Z
LAST-MODIFIED:20260224T214651Z
UID:20376-1775692800-1775865599@ntint.com
SUMMARY:PDA West Coast Chapter - Digital Transformation
DESCRIPTION:Join Us at PDA West Coast Chapter: Digital Transformation\n  \nWhitney French will be attending this upcoming event hosted by PDA West Coast Chapter in Las Vegas\, bringing together professionals across diagnostics\, medical devices\, and digital health.\n  \nThe program highlights emerging technologies\, regulatory considerations\, and practical strategies shaping the future of connected health solutions.\n  \nWhitney will be onsite and ready to answer questions about how to start reducing risk early in development — helping teams build stronger\, more compliant\, and resilient programs.\n  \nIf you’re attending\, please introduce yourself. She looks forward to connecting and discussing your goals.\n  \nRegister Here: https://www.pda.org/global-event-calendar/event-detail/pda-west-coast-chapter-devices-for-diagnostics-digital-health\n  \nLearn about how to reduce risk: https://ntint.com/
URL:https://ntint.com/event/pda-west-coast-chapter-digital-transformation/
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/11.-PDA-WCC-Digital-Transformation.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260407
DTEND;VALUE=DATE:20260408
DTSTAMP:20260606T050131
CREATED:20260226T175346Z
LAST-MODIFIED:20260226T185503Z
UID:20381-1775520000-1775606399@ntint.com
SUMMARY:PDA SouthEast - Spring Conference 2026
DESCRIPTION:Novatek International’s Gregory Froundjian will be attending the PDA Southeast Chapter: 2026 Spring Conference on April 7\, 2026\, in Tampa\, FL!\nRegister Here: https://www.pda.org/global-event-calendar/event-detail/pda-southeast-chapter-2026-spring-conference\nThis dynamic event brings together pharmaceutical quality and manufacturing professionals for a day of insightful educational sessions\, valuable networking opportunities\, and industry-leading discussions. The conference’s theme\, “Breaking the Mold – Advancing the Future of Pharma\,” focuses on how thoughtful innovation\, science-based approaches\, and risk-based thinking can drive the future of pharmaceutical quality beyond traditional compliance.\n\nAttendees will explore emerging technologies\, quality risk management strategies\, and modern tools shaping the industry—making this a must-attend gathering for innovators and quality leaders in pharma.\n\nIf you’re there too\, let’s connect! Looking forward to engaging conversations and meaningful collaboration across the industry.
URL:https://ntint.com/event/pda-southeast-spring-conference-2026/
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/10.-PDA-SE-Spring-Conference.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260324
DTEND;VALUE=DATE:20260326
DTSTAMP:20260606T050131
CREATED:20260220T155523Z
LAST-MODIFIED:20260226T185413Z
UID:20359-1774310400-1774483199@ntint.com
SUMMARY:Concept Heidelberg - GMP Pharma Congress
DESCRIPTION:GMP Pharma Congress\nSee you in Germany at the 28th Conference and Expo – Pharma Manufacturing & Technology\n  \nBe sure to introduce yourself to Sarah Alimirzaei and Agnes Barti to learn more about how the industry is changing and how to digitalize your system to exceed the new standards. \n  \nRegister Here: https://www.pharma-congress.com/\n  \nEvent Objective\nThis conference provides practical insights into the design\, construction\, qualification\, and operation of GMP-compliant pharmaceutical facilities. Participants will learn how to identify typical compliance risks\, implement effective clean room and containment concepts\, and align GMP and occupational safety requirements. Real-life case studies and expert presentations illustrate how regulatory expectations can be translated into GMP-compliant solutions. \n  \nBackground\nA GMP-compliant pharmaceutical facility provides the structural and organisational framework for manufacturing high-quality medicines. Clean Rooms play a central role by ensuring controlled environments that minimise particulate and microbial contamination. Regulatory authorities define detailed requirements for design\, operation and maintenance. Common compliance gaps include inadequate cleaning\, insufficient control of personnel and material flows and incomplete documentation. \nMany GMP problems originate already during the planning and construction phase. The design must anticipate regulatory expectations\, future workflows\, and technical interfaces – making project management a critical success factor. Cost\, schedule\, and GMP compliance must be balanced from concept to commissioning and qualification. \nIn addition to GMP\, occupational safety is equally important in the planning and operation of manufacturing facilities. GMP and occupational safety have become closely linked with the introduction of the PDE/ADE concept\, both aiming to prevent the release of active substances. While GMP focuses on avoiding cross contamination\, Environment\, Health & Safety ensures that employees are not exposed to harmful levels. Effective contamination control strategies therefore address both aspects. \nEnsuring clean room and facility compliance requires a coordinated approach across engineering\, quality\, and production – with inspections and audits placing growing emphasis on risk-based thinking and data integrity. \nThis conference presents practical examples of how these requirements can be effectively implemented.
URL:https://ntint.com/event/concept-heidelberg-gmp-pharma-congress/
LOCATION:RheinMain CongressCenter\, Friedrich-Ebert-Allee 1\, Wiesbaden\, 65189\, Germany
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/09.-Concept-Heidelberg-GMP-Pharma-Congress.jpg
ORGANIZER;CN="Concept Heidelberg GmbH":MAILTO:info@concept-heidelberg.de
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260322
DTEND;VALUE=DATE:20260328
DTSTAMP:20260606T050131
CREATED:20260219T185058Z
LAST-MODIFIED:20260219T185409Z
UID:20343-1774137600-1774655999@ntint.com
SUMMARY:PDA Week 2026
DESCRIPTION:Looking forward to PDA – Parenteral Drug Association Week 2026! \nVisit our booth #329 and discover how we’re shaping the future of parenteral drug development. \nCome meet our team:\nVicky Azadian\nIlona Endisch \n22-27 March 2026 | Denver\, CO \nRegister: HERE \nCelebrating PDA’s 80th and 20th anniversaries\, PDA Week 2026 brings together industry leaders and innovators from around the globe to explore the latest in pharmaceutical science\, technology\, and regulatory advancements. With a dynamic program filled with best practices and forward-looking insights\, PDA members have a chance to deepen their professional skills and expertise. \nPDA Week highlights include:\n\nPlenary and concurrent sessions\nRoundtables\, Mini-Workshops\, and Mini-Training Courses\nFast-paced lightning talks\nDirect connections with experts and peers\n\nExhibitors\, sponsors\, and posters in the Exhibit Hall \n\nSocial and networking events\, including Monday evening’s Opening Reception\nTechnical Report Live (TRL) watch parties\nOpportunities to meet presenters one-on-one\n\nIt’s the must-attend event for anyone in the industry—delivering a 360° update on all things pharma.
URL:https://ntint.com/event/pda-week-2026/
LOCATION:Gaylord Rockies\, 6700 N Gaylord Rockies Boulevard\, Denver\, CO\, 80019\, United States
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/02/08.-PDA-Week.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/Denver:20260319T160000
DTEND;TZID=America/Denver:20260319T200000
DTSTAMP:20260606T050131
CREATED:20260219T201218Z
LAST-MODIFIED:20260226T185256Z
UID:20351-1773936000-1773950400@ntint.com
SUMMARY:ISPE Rocky Mountain - Vendor Show
DESCRIPTION:Meet us the ISPE Rocky Mountain Vendor show on March 19 @ 4:00 pm – 8:00 pm! \n  \nVicky Azadian will be on-site to introduce you to key industry points that will push you to the top of the leaderboard. \n  \nDon’t forget to ask for her expertise on gaining traction and proving yourself in the industry. \n  \nRegister Here: https://rmispe.org/event/2026-vendor-show
URL:https://ntint.com/event/ispe-rocky-mountain-vendor-show/
LOCATION:The Limligh Hoel\, 1295 University Ave\, Boulder\, CO\, 80302\, United States
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/06.-ISPE-Rocky-Mountain-Vendor-Show.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260319
DTEND;VALUE=DATE:20260321
DTSTAMP:20260606T050131
CREATED:20260220T153532Z
LAST-MODIFIED:20260226T185117Z
UID:20355-1773878400-1774051199@ntint.com
SUMMARY:KENX - Validation University
DESCRIPTION:We’ll meet you in Philadelphia on March 19-20! \n  \nBe sure to attend Susan Cleary‘s talk on Digitalization Of Cleaning Validation Management! \nKalid Kassaby will also be there to introduce you to key points which would upgrade your position in the industry. (Kalid Kassaby | LinkedIn) \n  \nDate: March 19-20\, 2026\nVenue: Wyndham Philadelphia Historic District + Virtual\nRegister Here: https://kenx.org/conferences/validation-university/\nPromo Code: NOVA200\n  \nHere are the Key Takeaways from Susan’s talk. \n\nUnderstand the fundamentals of cleaning validation and its regulatory importance in ensuring product safety\, quality\, and compliance with GMP requirements.\nIdentify the limitations of traditional paper-based cleaning validation systems\, including inefficiencies\, data integrity risks\, and compliance challenges.\nExplore how digital tools improve cleaning validation management\, including automated workflows\, electronic records\, and real-time monitoring.\nLearn how digitalization enhances data integrity\, traceability\, and audit readiness through secure\, centralized\, and compliant data management systems.\nDiscover best practices and key considerations for implementing digital cleaning validation solutions\, including change management\, system validation\, and regulatory alignment.
URL:https://ntint.com/event/kenx-validation-university/
LOCATION:Wyndham Philadelphia Historic District\, 400 Arch Street\, Philadelphia\, 19106\, United States
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2026/02/07.-KENX-Validation-University.png
ORGANIZER;CN="KENX":MAILTO:info@kenx.org
GEO:39.9518939;-75.1473609
X-APPLE-STRUCTURED-LOCATION;VALUE=URI;X-ADDRESS=Wyndham Philadelphia Historic District 400 Arch Street Philadelphia 19106 United States;X-APPLE-RADIUS=500;X-TITLE=400 Arch Street:geo:-75.1473609,39.9518939
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260303
DTEND;VALUE=DATE:20260305
DTSTAMP:20260606T050131
CREATED:20260219T193716Z
LAST-MODIFIED:20260219T193716Z
UID:20348-1772496000-1772668799@ntint.com
SUMMARY:A3P - Aseptic Process & Low Bioburden
DESCRIPTION:Come meet Aram Montazami and Mélanie Rose at Aseptic and Low Bioburden Processes.\n\nWith a focus on Control\, Innovation and Compliance with Annex 1\n\n📅 March 3–4\, 2026\n📍 Beau-Rivage Palace\, Lausanne (Switzerland)\n\nThe EU GMP Annex 1 places contamination control and aseptic process performance at the forefront of pharmaceutical manufacturing priorities. The A3P Congress 2026 will dedicate two full days to aseptic and low bioburden processes\, bringing together experts\, industry leaders and regulatory representatives to discuss compliance\, innovation and operational excellence.\n\nKey topics will include:\n\nAseptic Process Simulation (APS): validation strategies\, best practices and case studies.\nProcess Improvement: new technologies\, automation and risk management to ensure robustness and consistency.\nEnvironmental Control: monitoring strategies and contamination control for both particulate and microbiological aspects.
URL:https://ntint.com/event/a3p-aseptic-process-low-bioburden/
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/05.-A3P-Switzerland-Aseptic-Process-Low-Bioburden.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260217
DTEND;VALUE=DATE:20260218
DTSTAMP:20260606T050131
CREATED:20260216T145834Z
LAST-MODIFIED:20260216T145834Z
UID:20339-1771286400-1771372799@ntint.com
SUMMARY:PDA West Coast Chapter - Quality Conference
DESCRIPTION:Come meet Whitney French at the upcoming PDA WCC Quality Conference Feb 17th. \nwhitney.french@ntint.com \n  \nGet ready to dive deep into the world of quality at this all-day conference – it’s going to be a game-changer! \n  \nJoin PDA West Coast Chapter\, industry leaders\, and quality professionals for a comprehensive\, full-day Quality Conference exploring the rapidly changing landscape of quality management. This conference is designed to equip professionals and organizations with the insights\, tools\, and strategies needed to stay compliant\, competitive\, and future-ready. \n  \nThroughout the day\, attendees will engage in expert-led presentations\, panel discussions\, and real-life case studies that showcase digital solutions and smarter inspection methodologies. Join us for a day of learning\, collaboration\, and innovation as we redefine what quality excellence looks like.
URL:https://ntint.com/event/pda-west-coast-chapter-quality-conference/
LOCATION:Gilead Scieces Inc.\, United States
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2026/02/03.-PDA-WCC-Quality-Conference.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251124
DTEND;VALUE=DATE:20251127
DTSTAMP:20260606T050131
CREATED:20251107T212004Z
LAST-MODIFIED:20251110T140443Z
UID:20269-1763942400-1764201599@ntint.com
SUMMARY:PharmaLab
DESCRIPTION:Join Parsa Famili’s talk on November 24-26 in Dusseldorf.\nCome find Sarah Alimirzaei on-site!\n  \nThe event for all pharmaceutical laboratory sectors will take place for the 13th time from 24-26 November 2025 – on site in Düsseldorf/Neuss. The PharmaLab 2025 conferences will cover various topics and lectures on analytics\, bioanalytics and microbiology. \nParallel to the conferences\, participants will have the opportunity to visit the accompanying trade exhibition. It offers comprehensive information about available products\, services and the latest developments around the laboratory. \n\n\nThe following conferences are part of PharmaLab on 25-26 November 2025: \n\nGMP Compliance Trends Analytical Laboratories\nNEW! Analytical Quality and Lifecycle Concepts\nLaboratory Optimization\, Automation and Digitalization\nNEW! Artificial Intelligence in Laboratories\nEndotoxin and Pyrogen Testing\nAlternative and Rapid Microbiological Methods\nCell and Gene Therapies/ ATMPs – Quality and Safety\nBioassays/Potency Assays – Regulatory Requirements\, Development and Routine Use\nNEW! Bioanalytical Control of Biological Drug Substances and Products
URL:https://ntint.com/event/pharmalab/
LOCATION:Crowne Plaza Düsseldorf / Neuss\, Dusseldorf\, Germany
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-PharmaLab-1.png
ORGANIZER;CN="Concept Heidelberg GmbH":MAILTO:info@concept-heidelberg.de
GEO:51.2011098;6.7235723
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251120
DTEND;VALUE=DATE:20251121
DTSTAMP:20260606T050131
CREATED:20251107T210537Z
LAST-MODIFIED:20251107T210537Z
UID:20261-1763596800-1763683199@ntint.com
SUMMARY:Délégation Quebec
DESCRIPTION:Trouvez Aram Montazami\, Mélanie Rose et Yara Massoud le 20 novembre à Paris.
URL:https://ntint.com/event/delegation-quebec/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-Delegation.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251119
DTEND;VALUE=DATE:20251121
DTSTAMP:20260606T050131
CREATED:20251107T211449Z
LAST-MODIFIED:20251107T211449Z
UID:20266-1763510400-1763683199@ntint.com
SUMMARY:Speak Pharma - 2nd Cleaning Process & Validation Conference
DESCRIPTION:Join Susan Cleary\, Ilona Endisch\, and Angel Ruiz on November 19-20 in Prague.\n  \nSpeak Pharma presents the 2nd edition\, scheduled in the beautiful city of Prague\, Czech Republic\, and online on November 19-20\, 2025. Industry leaders will explore critical aspects of safe pharmaceutical manufacturing\, “equipment design for rapid and robust CIP (Clean in Place) cleaning\, practical standards in cleaning validation\, and more. Part of the conference program will include in-person training by Igor Gorsky on ASTM standards. Gain insights from real-world cases and expert guidance on developing robust cleaning validation plans\, applying the QRM approach to cleaning\, and understanding how risk assessments impact product quality. Participate in interactive discussions to enhance your knowledge and practices. Secure your spot now by submitting a request. \nOur Focus \n\nImpact of Annex 1 on Cleaning Validation\nQRM Approach in Cleaning\nMaintaining Risk Analysis and Evaluation\nEquipment Designed for Cleanability\nPractical Cleaning Process Development\nRobust Cleaning Control Strategies and Compliance\nASTM Standards to Support Cleaning Process and Validation\nSustainability and Resource Efficiency\nDigital Transformation and Data Integrity\nCleaning Validation in HPAPI Manufacturing Facilities
URL:https://ntint.com/event/speak-pharma-2nd-cleaning-process-validation-conference/
LOCATION:Grandium Hotel Prague – Politickych veznu 913/12110 00 Prague 1\, Czech Republic
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-SpeakPharma.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251119
DTEND;VALUE=DATE:20251121
DTSTAMP:20260606T050131
CREATED:20251107T210947Z
LAST-MODIFIED:20251107T210947Z
UID:20263-1763510400-1763683199@ntint.com
SUMMARY:KENX - AI in GxP Europe
DESCRIPTION:Join Parsa Famili and Niccolo Moreno on November 19-20 in Dublin\, Ireland.\n  \n\nWelcome to Harness the Power of AI in GxP Europe\n\n\nUse Cases\, Process Optimization\, and Validation\, in beautiful Dublin\, Ireland! \nNovember 19-20\, 2025 | Dublin\, Ireland \n\n\nJoin us for an immersive 2-day event focused on leveraging and validating Artificial Intelligence (AI) to drive innovation and efficiency within the GxP environment. “Harness the Power of AI in GxP” will feature a series of case study driven sessions that reveal the latest developments in AI applications\, process optimization\, validation\, and compliance within regulated life sciences industries. Whether your goal is to validate AI for regulatory compliance\, streamline manufacturing\, or ensure data integrity\, this conference delivers actionable insights to keep you at the forefront of technology and regulation. \n\n\nSession Highlights: Dive into Real-World Use Cases and Compliance Strategies\n\n\nUnderstanding Regulatory Frameworks for AI in GxP\n\n\nExplore essential regulatory considerations\, including FDA guidance on AI\, Part 11 compliance for electronic records\, and the latest on data integrity standards. Industry experts will provide insights into ISPE® AI quality and compliance initiative and discuss how to ensure alignment with global standards. \n\n\n\nNavigating FDA guidance on AI/ML in life sciences\nPart 11 compliance: Ensuring secure and accurate electronic records\nISPE® AI Quality and Compliance Initiative: An in-depth overview\nAddressing data integrity challenges in AI-driven processes\nManaging regulatory expectations across global markets\nEnsuring transparency and accountability in AI validation processes\n\n\n\nCase Studies and Validation of AI in GxP\n\n\nLearn from specific use cases demonstrating how AI is transforming GxP processes. Topics include optimizing manufacturing workflows\, enhancing validation accuracy\, and applying predictive analytics in quality control. Sessions will also cover best practices for validating AI processes to meet compliance requirements\, ensuring safe and effective AI implementation in regulated environments. \n\n\n\nAI-driven automation in GMP environments: Practical examples\nOptimizing quality control and data integrity through AI\nBest practices for validating AI algorithms and models\nLeveraging predictive analytics for preventive maintenance\nCase study: AI applications in continuous process improvement\nEnhancing validation speed and accuracy with AI\nReal-world applications of AI in manufacturing and supply chain
URL:https://ntint.com/event/kenx-ai-in-gxp-europe/
LOCATION:Hyatt Centric DUBLIN\, IRELAND\, Dublin\, Ireland
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-KENX-AI-in-GxP-Dublin.png
ORGANIZER;CN="KENX":MAILTO:info@kenx.org
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251118
DTEND;VALUE=DATE:20251119
DTSTAMP:20260606T050131
CREATED:20251107T205938Z
LAST-MODIFIED:20251107T210018Z
UID:20258-1763424000-1763510399@ntint.com
SUMMARY:A3P - Digitalization
DESCRIPTION:Join Parsa Famili\, Niccolo Moreno and Angel Ruiz in Barcelona on Nov 18th\nThis A3P conference will bring together industry experts from the pharmaceutical sector to explore the challenges and opportunities of digitalization.\n\nA full day dedicated to delving into the regulatory aspects of Annex 11\, as well as in-depth sessions on alarm review\, the digitalization of cell therapy\, and warehouse automation.\nIn addition\, we will host a round table to analyze synergies and emerging use cases.\n\nThis event offers a rigorous and practical approach\, ideal for quality\, production\, and engineering teams seeking to understand and adopt innovative digital strategies.\n\nAnother intense day to share experiences\, discuss solutions\, and continue building together the pharmaceutical Industry 4.0.
URL:https://ntint.com/event/a3p-digitalization/
LOCATION:Renaissance Barcelona Fira Hotel\, Barcelona\, Spain
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-A3P-Digitalization.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251112
DTEND;VALUE=DATE:20251114
DTSTAMP:20260606T050131
CREATED:20251107T204231Z
LAST-MODIFIED:20251107T204231Z
UID:20240-1762905600-1763078399@ntint.com
SUMMARY:Growth Day Direct - Daiichi-Sankyo & Rapid Micro Biosystems
DESCRIPTION:Join Sarah Alimirzaei at Growth Day Direct\, Nov 12-13 in Munich\, Germany.\n\nMany of the world’s leading pharma companies will showcase scientific presentations\, guest speakers\, and shared insights at this exclusive two-day event hosted by Daiichi Sankyo and Rapid Micro Biosystems.\n\n\n\n\nReserve your seat today for our event taking place at the Munich Airport Marriott Hotel\, Alois-Steinecker-Strasse 20\, Freising\, Germany on November 12–13\, 2025! This is your ideal opportunity to network with other quality control professionals and get practical\, real-world answers to your questions about the Growth Direct® System for Sterility\, EM\, Water\, and Product Bioburden Testing.
URL:https://ntint.com/event/growth-day-direct-daiichi-sankyo-rapid-micro-biosystems/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-Growth-Day-Direct.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251107
DTEND;VALUE=DATE:20251108
DTSTAMP:20260606T050131
CREATED:20251107T205330Z
LAST-MODIFIED:20251107T205504Z
UID:20256-1762473600-1762559999@ntint.com
SUMMARY:PDA West Coast Chapter - Quality Ball
DESCRIPTION:Join Parsa Famili and Whitney French at the Quality Ball in San Francisco Nov 7th\n  \nPlease join us for the PDA West Coast Chapter’s 2025 Quality Ball located at the California Academy of Sciences\, a renowned research institute and natural history museum located in San Francisco’s Golden Gate Park. The event will be focusing on the critical intersection of quality\, compliance\, and innovation in today’s rapidly evolving industries. This thought-provoking gathering will explore how these three areas can work in harmony to overcome challenges\, drive success\, and improve outcomes in today’s industry. \nAs new technologies emerge\, innovation plays a crucial role in advancing quality improvements and enabling more efficient\, effective ways of working. But how do we balance the drive for cutting-edge solutions with the rigorous demands of quality and compliance? This event will dive deep into the synergies—and tensions—between these three forces\, while also addressing the challenges that regulations can place on technological advancement. \nOur expert speakers will share valuable insights: \n\nHow innovation can act as a catalyst for enhancing quality\nHow organizations can strike the right balance between pushing the envelope and staying compliant\nThe complexities of integrating all three areas into a cohesive strategy\nReal-world challenges faced in the quest for innovation\nHow they’ve overcome hurdles to ensure compliance and maintain the highest standards of quality\n\nJoin us for an interactive panel discussion with experts and peers\, as we uncover the latest trends and approaches that are shaping the future of quality\, compliance\, and innovation. Don’t miss this opportunity to connect\, collaborate\, and learn from the best in the industry! Whether you’re navigating regulatory requirements in a new market or striving to bring breakthrough technologies to life\, this event will provide you with the knowledge and strategies you need to thrive in today’s complex landscape.
URL:https://ntint.com/event/pda-west-coast-chapter-quality-ball/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/11/Novatek-X-PDA-WCC-Quality-Ball.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251027
DTEND;VALUE=DATE:20251030
DTSTAMP:20260606T050131
CREATED:20251007T184353Z
LAST-MODIFIED:20251007T184353Z
UID:20224-1761523200-1761782399@ntint.com
SUMMARY:PDA - Pharmaceutical Microbiology Conference 2025
DESCRIPTION:The PDA Pharmaceutical Microbiology Conference 2025 marks two decades of advancing microbiological science and practice. This milestone event brings together the global microbiology community\, including experts from industry\, academia\, and regulatory agencies\, to explore the evolving landscape of pharmaceutical microbiology. This year’s theme\, Microbial Resilience: Today’s Response\, Tomorrow’s Plan\, reflects our focus on navigating present-day challenges while building robust strategies for the future.
URL:https://ntint.com/event/pda-pharmaceutical-microbiology-conference-2025/
LOCATION:Grand Hyatt Washington\, 1000 H St NW\, WA\, United States
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/10/Novatek-X-PDA-Microbiology.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20251022T070000
DTEND;TZID=UTC:20251022T090000
DTSTAMP:20260606T050131
CREATED:20251009T181030Z
LAST-MODIFIED:20251009T181147Z
UID:20228-1761116400-1761123600@ntint.com
SUMMARY:Webinar: Risk-Based Quality Information Management
DESCRIPTION:Join us on October 22nd (7:00am – 9:00am EST) for an in-depth webinar focused on Risk-Based Quality Information Management. \nCorinne Cleary and Merle Eloise will speak on different issues companies face in Quality Information Management and they’ll discuss the exploration of various solutions to mitigate the risks involved. \nClick the link below to register: \nhttps://attendee.gotowebinar.com/register/5608412450938833502
URL:https://ntint.com/event/webinar-risk-based-quality-information-management/
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/10/Novatek-Webinar-Middle-East.png
LOCATION:https://attendee.gotowebinar.com/register/5608412450938833502
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251014
DTEND;VALUE=DATE:20251015
DTSTAMP:20260606T050131
CREATED:20251007T154816Z
LAST-MODIFIED:20251009T182835Z
UID:20221-1760400000-1760486399@ntint.com
SUMMARY:Particle Measuring Systems - Discover the future of automated environmental monitoring in Pharma
DESCRIPTION:Novatek International is excited to partner with Particle Measuring Systems for a webinar that dives deep into how environmental monitoring in pharmaceutical manufacturing is being transformed. Join us on October 14\, 2025 for “Discover the Future of Automated Environmental Monitoring in Pharma.” \n  \nWhat we’ll cover: \n💠How to design automated\, paperless workflows that reduce human error and increase data integrity. \n💠Regulatory compliance paired with new digital tools to manage\, trend\, and validate environmental data. \n  \n🎙️ Speakers include Susan Cleary\, Director of Product Development at Novatek International\, with 25 years in quality\, compliance\, and contamination control — and Marc Machauer\, Global OEM Coordinator at Particle Measuring Systems\, expert in aseptic line design and cleanroom control. \n  \n👉 Don’t miss this chance to see what today’s validated systems can do for your facility—faster implementation\, stronger compliance\, and fewer manual interventions. \n  \nRegister here: https://www.pmeasuring.com/webinar/discover-the-future-of-automated-environmental-monitoring-in-pharma/
URL:https://ntint.com/event/particle-measuring-systems-discover-the-future-of-automated-environmental-monitoring-in-pharma/
ATTACH;FMTTYPE=image/jpeg:https://ntint.com/wp-content/uploads/2025/10/PMS-webinar.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251013
DTEND;VALUE=DATE:20251015
DTSTAMP:20260606T050131
CREATED:20251007T144050Z
LAST-MODIFIED:20251007T144050Z
UID:20213-1760313600-1760486399@ntint.com
SUMMARY:PDA (APAC) - Aseptic Manufacturing Excellence Conference 2025
DESCRIPTION:
URL:https://ntint.com/event/pda-apac-aseptic-manufacturing-excellence-conference-2025/
LOCATION:Pullman Melboure on the Park\, 192 Wellington Parade\, East Melbourne\, Victoria\, 3002\, Australia
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/10/Novatek-X-PDA-APAC-Australia.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20251009
DTEND;VALUE=DATE:20251011
DTSTAMP:20260606T050131
CREATED:20250909T161737Z
LAST-MODIFIED:20250910T182324Z
UID:20184-1759968000-1760140799@ntint.com
SUMMARY:KENX - GMP University
DESCRIPTION:Don’t forget to use our discount code: NOVA200 \nOur SME (Subject Matter Expert) Sheba Zaman will be available to answer all your questions about upgrading compliance of your process. \n  \nGMP University 2025 takes a deeper dive into advanced GMP topics and the latest industry trends. This two-day conference in La Jolla\, CA is designed for professionals who want to stay at the forefront of Good Manufacturing Practices\, explore new technologies\, and learn how to implement best practices for regulatory compliance and operational excellence. \nWhat You’ll Gain: \nGMP University 2025 focuses on emerging challenges and innovations in the GMP landscape\, offering insights into the future of compliance and quality assurance. Key topics include: \n\nModernizing Quality Systems: Learn about the latest approaches to building resilient and agile quality systems that adapt to regulatory changes.\nDigital Transformation in GMP: Discover how automation\, data analytics\, and digital tools are reshaping GMP processes\, from documentation to quality control.\nRisk Management & Continuous Improvement: Explore advanced risk management strategies that support continuous improvement and help maintain compliance.\nSupplier & Supply Chain Management: Gain insights into GMP compliance across global supply chains\, including supplier qualification and risk mitigation.\nRegulatory Updates & Compliance: Stay informed about current and upcoming regulatory changes and understand what they mean for your operations.\n\nEvent Highlights: \n\nExpert-Led Sessions & Case Studies: Participate in in-depth presentations and case studies from industry leaders who are innovating in GMP.\nWorkshops & Hands-On Learning: Take part in interactive workshops that focus on applying new GMP trends and best practices in real-world scenarios.\nPanel Discussions & Roundtables: Join discussions with experts on hot topics like digital compliance\, quality metrics\, and regulatory expectations.\nNetworking with Industry Leaders: Connect with peers\, vendors\, and key opinion leaders to share insights\, explore challenges\, and build partnerships.\n\n 
URL:https://ntint.com/event/kenx-gmp-university/
LOCATION:San Diego Marriot La Jolla\, 4240 La Jolla Village Drive\, La Jolla\, CA\, 92037\, United States
ATTACH;FMTTYPE=image/png:https://ntint.com/wp-content/uploads/2025/09/Novatek-X-KENX-GMP-University-San-Diego.png
ORGANIZER;CN="KENX":MAILTO:info@kenx.org
END:VEVENT
END:VCALENDAR