Now launching: meet Scilife’s Design & Development tool for medical devices

🩺 Launching a medical device to market? Early design control helps you avoid last-minute chaos and compliance walls. Join our 30’ webinar to meet Scilife’s Design & Development solution.
🚀 Don’t reverse-engineer compliance. Build it in.
We’ve seen this scenario plenty of times. Medtech teams racing to launch a life-changing device, only to hit a compliance wall. Documentation is skipped, QA comes in too late, and delays ensue…
To help you stay on track and simplify design control from day one, we’re launching Scilife’s brand new Design & Development solution. Join our 30-minute live session to find out more.
You will learn about:
- Ensuring ISO 13485:2016 and FDA 21 CFR 820 compliance by documenting design controls with industry-aligned workflows.
- Spot gaps with the auto-generated traceability matrix, link project elements, and reduce manual work.
- Centralize design and stay audit-ready with version control, audit trails, and streamlined approvals.
You will hear from Judith San Juan, Product UX UI Designer at Scilife, who will be introducing the new feature. Angel Buendía, our Knowledge Manager, will be moderating this session.
📅 July 8th, 2025 | 11:00H (CEST)
No need to recreate history during audits. Build once, with ease and compliance in mind, including quality from the start.