Fast GxP Compliance

    Fast GxP compliance (3)

    Webinar on demand

    Fast GxP Compliance

    Implementing and Validating ERP Systems Under GxP

    Life sciences companies must digitalize fast while staying GxP compliant. In this joint webinar, QbD Group and delaware show how SAP technology and proven validation frameworks make rapid, compliant digital transformation possible.

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    On demand

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    1h

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    Life Sciences

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    English

    Accelerate digital transformation while staying compliant

    Digital transformation in life sciences is accelerating. But implementing systems like SAP S/4HANA or MES within a GxP-regulated environment remains complex, time-consuming, and validation-heavy.

    In this session, delaware and QbD Group will share how their combined expertise enables a pragmatic, validated approach toimplementing and validating SAP systems faster and more efficiently within regulated life sciences environments.

    What you'll learn

    • Best practices forSAP implementation under GxP
    • How to avoid common pitfalls in validation and CSV
    • Insights into ourjoint validation methodology and accelerators
    • Real-world examples where innovation meets compliance

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    Who should attend?

    This webinar is designed for professionals in the Pharmaceutical, Biotech, and MedTech industries, including:

    • IT & Digital Transformation Leaders
    • Quality & Compliance Experts (QA / CSV / RA / IT)
    • Project Managers involved in SAP or system implementations

    Learn from our experts

    Speakers

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

    Jonathan Boel (1)

    Jonathan Boel

    Division Head Software Solutions & Services at QbD Group

    Jeroen Leemen

    Jeroen Leemen

    Software Validation Expert at QbD Group

    Evelien cools - delaware

    Evelien Cools

    Industry Lead Life Sciences at delaware

    About the hosts

    QbD Group supports life sciences companies worldwide in achieving the highest quality and safety standards, from idea to patient, with expertise in quality assurance, regulatory compliance, clinical services, and digital solutions.

    delaware is a global consultancy and SAP Platinum Partner, guiding organizations through their business and digital transformations with end-to-end IT and enterprise technology solutions.

    Together, we help life sciences companies bridge the gap between technology and compliance — ensuring every digital initiative is validated, inspection-ready, and future-proof from day one.

    delaware x qbd

    Fast GxP compliance (2)

    Our support

    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.

    Our digitalization solutions

    Accelerate your digital transformation

    Through our strategic partnership with delaware, we combine deep life sciences expertise with best-in-class digital technologies. Together, we help organizations implement powerful systems like SAP, fully validated, compliant, and aligned with your processes from day one.

    • Faster time-to-value

    Accelerate digital transformation without delays from compliance bottlenecks, while ensuring full regulatory assurance.

    • Inspection-ready systems

    Every solution is validated and audit-proof from day one.

    • Reduced risk

    Avoid common pitfalls in system validation and regulatory misalignment.

    • Operational excellence

    Drive efficiency through integrated, compliant digital systems.

    Resources you might find interesting

    Whitepaper - Digitalization in the Pharmaceutical Industry - Software Solutions & Services

    Digitalization in the Pharmaceutical Industry: And How to Stay Compliant

    Digitalization and Pharma 4.0 drive digital transformation. Explore the role of CSV in pharma's digital journey.

    Download whitepaper

    CSV & Digitalization FAQ

    The Essential CSV & Digitalization FAQ for Life Sciences Companies

    Get answers to real CSV questions from clients and experts. Download our FAQ to stay compliant, audit-ready, and confident in your validation strategy.

    Download FAQ

    QMS pre-implementation and validation

    Case Study - Building a Unified QMS for a Non-Profit Lab Organization

    A non-profit lab improved compliance and efficiency by unifying quality management through a validated SaaS QMS across all departments.

    Read client case

    Life Sciences Digitization Your Compliance Roadmap

    Life Sciences Digitization: Your Compliance Roadmap

    Discover how life sciences digitization boosts efficiency, ensures data integrity, and strengthens compliance. Partner with QbD experts for your roadmap.

    Read blog

    Discover all

    We share the latest news

    Staying on top of the latest in the life science industry can be a daunting task. This newsletter will keep you up-to-date with the latest news, blogs and webinars so you can keep ahead of the curve.

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