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

Fast GxP Compliance

Accelerating Digital Transformation in Life Sciences

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

Learn how to implement and validate SAP efficiently, without compromising on compliance.

Learn more

21 January

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.

This session will introduce a proven framework for accelerating compliant SAP implementations, built on a standardized GAMP® 5-aligned methodology that minimizes customization and validation overhead while ensuring compliance from day one.

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

This webinar is designed for IT, QA, and Compliance leaders in pharma, biotech, and MedTech, along with project managers leading SAP or digital transformation initiatives, and CSV/QA professionals responsible for validation in GxP environments.

Register here

Our Fast GxP Compliance Approach

Built around three pillars:

Process-Centric Validation: Align validation with critical business processes and risk levels.
Continuous Validation: Maintain compliance dynamically throughout the lifecycle.
Predefined User Stories: Use industry-specific assets to cut validation time and cost.

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

Senior Manager Life Sciences at delaware

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

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

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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