How to Streamline eQMS Validation Without Sacrificing Compliance
Includes a Live Web Event on 10/22/2026 at 1:00 PM (EDT)
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For many Quality teams, software validation has become synonymous with mountains of documentation and endless testing. Add AI features into the mix, and it's easy to see why validation can feel more complicated than ever.
But it doesn’t have to be.
In this session, we'll explore how Computer Software Assurance (CSA) is changing the way regulated organizations approach software validation. You'll learn how to replace excessive documentation with a streamlined, risk-based approach that keeps compliance front and center while cutting out unnecessary effort. We'll also discuss where software vendors can – and should – help lighten the validation workload, and how the same CSA principles can help you confidently validate AI-enabled software as these technologies become part of everyday quality operations.
Attendees will learn how to:
- Apply CSA principles to focus validation where it matters most.
- Understand how vendors and customers can share responsibility for a more efficient validation process.
- Approach AI-enabled software with a validation strategy that supports innovation without compromising compliance.
Thank you to ZenQMS for sponsoring this webinar!
Luiggi Colan
Senior QA & Training Specialist
ZenQMS
Luiggi Colan is a Quality Assurance and Training professional with deep experience in quality systems, regulatory readiness, and software validation across the life sciences space. Earlier in his career, he held a Research and Development Associate role at Axalta and technical writing and sterility assurance roles at WuXi Advanced Therapies. He has been with ZenQMS since 2021 and currently serves as Senior QA and Training Specialist, supporting quality and compliance across the organization. Luiggi specializes in 21 CFR Part 11, EU Annex 11, HIPAA, and GDPR compliance, as well as GAMP 5 software validation. He also works extensively with ISO 9001, ISO 27001, and SOC 2 and CSA frameworks.
