Upcoming webinar | 21 January 2026 | 10:30 AM CET

Fast GxP Compliance

Accelerating Digital Transformation in Life Sciences

Life sciences companies face a dual challenge: the need to digitalize while meeting stringent GxP requirements. How can you achieve both, without compromising quality or compliance?

QbD Group and delaware are joining forces to present a free webinar combining delaware’s deep technology and SAP expertise with QbD’s strong foundation in regulatory compliance, validation, and data integrity.

Learn more

21 January - 10:30 AM CET

45 min + Live Q&A

Pharma, Biotech & MedTech

English

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 to implementing and validating SAP systems faster and more efficiently within regulated life sciences environments.

What you'll learn

Best practices for SAP implementation under GxP
How to avoid common pitfalls in validation and CSV
Insights into our joint validation methodology and accelerators
Real-world examples where innovation meets compliance

Register here

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

Division Head Software Solutions & Services at QbD Group

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

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

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

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

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

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

Read blog

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