Traceability from day one: Smarter design controls with Scilife
Your device is ready, but scattered docs & missing traceability risk delaying approval.
Discover how Scilife’s Design & Development keeps you audit-ready and submission-ready.
After investing heavily into your new device, pre-market submissions are around the corner… Only to realize compliance has been entirely overlooked. Scattered documents, missing design decisions, broken traceability, risking a failed submission and costly market delays.
During our upcoming webinar, you’ll learn how Scilife's Design and Development helps you stay audit-ready by organizing design controls, ensuring traceability and avoiding compliance walls.
You’ll learn how to:
- Streamline design control documentation in line with ISO 13485:2016 and FDA 21 CFR Part 820
- Instantly spot gaps with an auto-generated traceability matrix
- Ensure proper approvals with 21 CFR Part 11-compliant e-signatures
- Keep teams aligned and on schedule with automated workflows
- Track changes, compare versions, and maintain a complete audit trail
You’ll hear from Laura Gilbert, Product Specialist, and Angel Buendía, Knowledge Manager, as they’ll show you how the Design and Development solution boosts innovation by removing compliance complexity.
📅 September 25th, 2025 | 11:00H (CEST)
Stay audit-ready from the start by building smarter, with compliance as a part of the process, not as a separate one.