Scilife Showcase | When nonconformities strike: how to stay compliant with Scilife

When traceability fails, small deviations can erupt into regulatory volcanoes. If you’re struggling to capture, investigate, and close failure events due to scattered data or manual records, it might be time to reboot your quality system.

Join this session to see how Scilife’s Events Solution ensures full traceability and compliance with ISO 13485:2016 and GMP—featuring a real-world case of a medical device manufacturer resolving a component failure through a connected digital workflow.

Showcase | When nonconformities strike: how to stay compliant with Scilife
November 25th, 2025 | 11:00H (CET)

You’ll learn how to:

• Record and classify deviations, nonconformities, or OOS results with traceable data.
• Attach evidence (images, reports, CoAs) for complete investigations.
• Assign owners, set timelines, and track progress automatically.
• Link events to CAPAs for a connected investigation process.
• Generate shareable reports with approvals and digital signatures.

You’ll hear from Jordi Ametller, Account Executive, and Angel Buendía, Knowledge Manager, as they show you how to use Scilife’s platform to successfully record, assess, investigate and revolve failure events, stress-free.

Register for free now

Join and get action-driven strategies to manage quality events the smart way.