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. Participants will learn best practices for SAP implementation under GxP, how to avoid common pitfalls in validation and CSV, and gain insights into joint validation methodologies and real-world examples where innovation meets compliance.
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.
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.
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.
向最优秀的人学习
Hear from industry experts who bring hands-on experience in implementing and validating systems in GxP-regulated environments.
Division Head Software Solutions & Services at QbD Group
Jonathan co-leads the Quality Assurance and Software Solutions & Services divisions at QbD Group. He is a CSV (Computer System Validation) expert who drives digital transformation and technology-enabled compliance solutions for the life sciences industry, including QbD's cloud-based pre-validated QMS and eIFU services.
Software Validation Expert at QbD Group
Jeroen is a Quality & Compliance Engineer at QbD Group. With a background in biomedical sciences, he specializes in software validation, GMP compliance, and data integrity across the pharmaceutical industry.
Industry Lead Life Sciences at delaware
Industry Lead Life Sciences at delaware, guiding customers in digital transformation from molecule to market. Specializes in elevating operational processes to best-in-class practices with strategic and pragmatic implementation approaches.
这是为您准备的吗？
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
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Digital transformation, data integrity, and AI/ML compliance solutions for the life sciences industry.
