Compliance at Risk: Why Manual Systems Fail Under Pressure
GMP compliance doesn’t belong in Excel.
Yet too many teams are still relying on spreadsheets, Word docs, and disconnected tools to manage critical quality processes.
The result?
❌ Poor traceability
❌ Uncontrolled changes
❌ Major compliance risks
Join our Showcase to discover how to move from outdated tools to a connected, audit-ready eQMS with Scilife.
Managing quality with spreadsheets, Word files, email threads, and other disconnected tools might seem manageable—until they fail.
And when they do, the consequences in a GMP-regulated environment can be severe.
Join us for a live Scilife Showcase where we’ll dive into the real compliance risks of manual systems and how you can address these risks once and for all with Scilife. No more uncontrolled changes, late CAPAs, or audit findings.
In this session, we’ll show you:
- The key compliance risks associated with manual quality systems
- What happens when these risks escalate into non-conformities
- Real-world regulatory cases that show how small process gaps became major issues
- Critical risk areas you might be exposed such as version control issues and more
- How an eQMS like Scilife systematically addresses compliance risks
You’ll hear from Jordi Ametller, Account Executive, and Angel Buendía, Knowledge Manager, as they break down these regulatory pitfalls and demonstrate how to eliminate them with a smarter approach to quality.
📅 June 17th, 2025 | 11:00H (CEST)
Don’t wait for a non-conformity to expose the cracks.
This is your moment to take control, tighten compliance, and leave manual messes behind, for good.