AI in Life Sciences
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Upcoming webinar | 19 March 2026 | 10:30 AM CET
AI in Life Sciences
Implementing Trustworthy, Compliant AI in a GxP Environment
Leveraging AI in life sciences is powerful, but also complex under GxP. In this joint webinar, QbD Group and delaware show how to implement AI in a trustworthy, validated, and inspection-ready way, with the right approach to data, explainability, and lifecycle management.
19 March - 10:30 AM CET
45 min + Live Q&A
Life Sciences
English
Implement AI faster without losing compliance
AI is accelerating digital transformation in life sciences. But implementing AI within a GxP-regulated environment introduces specific risks, especially when data is spread across multiple systems and processes.
Without the right foundations, organizations face challenges like inconsistent data, missing audit trails, and traceability gaps. At the same time, model transparency and explainability are increasingly scrutinized during audits. And because AI models evolve over time, a robust lifecycle management approach, aligned with CSA principles, becomes essential.
In this interactive webinar, QbD Group and delaware share how their combined expertise enables a pragmatic, integrated, and validated approach to implementing AI in regulated life sciences environments, so you can move from proof-of-concept to compliant deployment with confidence.
What you'll learn
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Best practices for AI implementation under GxP
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How to avoid common pitfalls, such as:
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Poor quality or insufficiently governed training/validation data
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Deploying black-box models with low explainability
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Applying insufficient governance and controls
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Insights into our joint framework methodology for compliant AI
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Real-world examples where innovation meets compliance
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)
- AI enthusiasts who want to go from proof-of-concept to implementation
Speakers
Hear from industry experts who bring hands-on experience in implementing and validating systems in GxP-regulated environments.
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Jonathan Boel
Division Head Software Solutions & Services at QbD Group
Evelien Cools
Industry Lead Life Sciences at delaware
Pieter Smits
Project Manager at QbD Group
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.
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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.
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
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.
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.
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.
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.
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.
