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    AI in Life Sciences

    Session 2, Your Questions Answered

    Adopting AI in life sciences holds enormous potential, but navigating GxP requirements adds real complexity. In this joint session, QbD Group and delaware walk you through how to deploy AI that is trustworthy, validated, and inspection-ready, covering data governance, explainability, and lifecycle management. Building on the first session, this edition dedicates more time to answering your questions, addressing the topics raised by the audience in Session 1, and opening the floor for live debate and discussion.

    miércoles, 13 de mayo de 2026
    3 PM CEST / 1 PM GMT
    Software Solutions & Services
    Español

    Implement AI faster without losing compliance

    AI is reshaping digital operations across life sciences. Yet deploying AI within a GxP-regulated environment brings distinct risks, particularly when data is distributed across disparate systems and workflows.

    Without solid foundations, organizations encounter hurdles such as fragmented data, gaps in audit trails, and limited traceability. Model transparency and explainability are also drawing increased regulatory attention during inspections. Moreover, because AI models continuously evolve, a structured lifecycle management strategy, aligned with CSA principles, is indispensable.

    This session covers the same core presentation as Session 1, but with a different focus: your questions take center stage. Rather than a one-way walkthrough, this is an open, interactive session built around debate, discussion, and answering the questions already raised in Session 1, as well as new ones from the live audience. If you attended the first session and left with unanswered questions, or if you're joining for the first time and want a more conversational format, this is the session for you.

    QbD Group and delaware present how their combined strengths deliver a pragmatic, integrated, and validated approach to AI adoption in regulated life sciences settings, helping you transition from proof-of-concept to compliant deployment with confidence.

    ¿Qué aprenderás?

    • Best practices for AI implementation under GxP
    • How to avoid common pitfalls, such as:
      • Poor quality or insufficiently governed training and validation data
      • Deploying black-box models with low explainability
      • Applying insufficient governance and controls
    • Insights into our joint framework methodology for compliant AI
    • Real-world examples where innovation meets compliance
    • Answers to your questions, both those raised in Session 1 and new ones submitted live

    Sobre los ponentes

    QbD Group partners with life sciences organizations across the globe to uphold the highest quality and safety standards, from concept to patient, leveraging expertise in quality assurance, regulatory compliance, clinical services, and digital solutions.

    delaware is a global consultancy and SAP Platinum Partner that helps organizations navigate business and digital transformation through comprehensive IT and enterprise technology solutions.

    Together, we enable life sciences companies to close the gap between technology and compliance, making sure every digital initiative is validated, inspection-ready, and future-proof from the start.

    Nuestro soporte

    Our expertise in software implementation, validation, and IT partnerships bridges the gap between regulatory requirements, business processes, and technology. Whether you want to modernize workflows, enhance data utilization, or future-proof your systems, we guide you every step of the way.

    Aprende de los mejores

    Ponentes

    Hear from industry experts who bring hands-on experience in implementing and validating systems in GxP-regulated environments.

    Jonathan Boel

    Jonathan Boel

    Division Head Software Solutions & Services at QbD Group

    Jonathan codirige las divisiones de Quality Assurance y Software Solutions & Services en QbD Group. Es un experto en CSV (Computer System Validation) que impulsa la transformación digital y las soluciones de cumplimiento habilitadas por tecnología para la industria de Life Sciences, incluyendo los servicios de QMS pre-validado en la nube y eIFU de QbD.
    Evelien Cools

    Evelien Cools

    Industry Lead Life Sciences at [delaware](https://www.delaware.pro/en-be)

    Industry Lead Life Sciences en delaware, acompaña a los clientes en la transformación digital desde la molécula hasta el mercado. Especializada en elevar los procesos operativos a las mejores prácticas con enfoques de implementación estratégicos y pragmáticos.
    Pieter Smits

    Pieter Smits

    Project Manager at QbD Group

    Pieter es Project Manager en QbD Group, donde coordina equipos multidisciplinares para llevar a cabo proyectos de consultoría en calidad y regulación.

    Comienza en

    26Days
    15Hours
    29Min
    38Sec

    Regístrate aquí

    ¿Es para ti?

    ¿A quién va dirigido?

    This webinar is tailored for professionals working in the Pharmaceutical, Biotech, and MedTech sectors, including: Learn from our experts

    IT & Digital Transformation Leaders

    Quality & Compliance Experts (QA, CSV, RA, IT)

    AI enthusiasts who want to go from proof-of-concept to implementation

    Anyone who attended Session 1 and wants their questions answered, or who prefers a more interactive format

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