Meet Scilife’s Design & Development tool - Form page

Products
Products

Smart QMS

Transform quality into your brightest asset

Smart QMS for Medical Devices

Accelerate from idea to market for medical devices

Controlled Printing and Reconciliation

21 CFR 11 compliant controlled printing

Self-guided tours >>

Take an interactive, self-guided tour to see how Scilife helps you manage quality

Featured capabilities

Document Management

Ensure a digitalized, quality-driven approach

Quality Events Management

Reduce compliance issues and save time

Change Control Management

Implement change faster

Risk Management

Take away the dread and reduce the risks

Quality KPIs

Enhance performance with quality metrics

Training Management

Boost continuous learning

CAPA Management

Streamline workflows to instill a quality culture

Audits Management

Remove stress and simplify compliance

Equipment Management

Ensure consistent maintenance
Solutions
Industries

Pharma and Biotech

Integrate and automate all your quality process

Medical Devices

Bring safe and compliant devices to market faster

Medicinal Cannabis

Boost efficiency to breeze through trial deadlines

CRO/CMO

Boost efficiency to breeze through trial deadlines

ATMP

Track all your manufacturing process

Use cases

Building a GMP-compliance QMS

Ensure quality and safety in all your products

Becoming audit ready

Stay audit-ready stress-free anytime

Streamline Design Control process

Ensure full traceability in your Medical Device

Complying with GDP standards

Safeguard your supply chain with GDP compliance

Platform

Security

Compliance

Integrations

Calculate your custom ROI

Curious about the ROI of implementing an eQMS? Get your ROI figure here >>

Schedule a Demo

Turn quality into your brightest asset with Scilife. Get started >>
Resources
Blog

Uncover our latest expert content

Glossary

Increase your quality terminology

Guides and Tools

Find all the guides and tools you need to succeed

Quality Management Soft Skills

Master the essential soft skills for a quality-driven life sciences team

Events and Webinars

Attend fascinating talks and workshops

Smart Quality Summit

Quality takes center stage—where it belongs

2025 Global Quality Outlook

Stay at the forefront of the latest trends

Scilife Academy

Your hub for continuous learning

How mature is your quality management?

Take the 4-minute scan and discover your quality maturity score >>

Want to improve your medical device QMS?

Our QARA guide has everything you need for medical device QMS. Dive in >>
Customers
Customer spotlights

Customer Stories

Read how companies switching to Scilife

Customer Resources

Scilife Academy

Build your skillset and learn best practices

Knowledge Base

Learn how to use Scilife and get answers to your questions.

Learn with Scilife Academy

Explore our product video lessons and discover how to get the most out of Scilife here >>
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Remote life, Scilife style!

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Pricing
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Get ready to simplify design control

This tool is designed to make compliance second nature, helping QA and product teams stay ahead of the curve and keep documentation organized, timely, and audit-ready.

What you’ll learn in this session:

Stay ISO 13485:2016 and FDA 21 CFR 820 compliant with industry-aligned design control workflows.
Use our traceability matrix to spot gaps, link project elements, and reduce manual work.
Ensure audit-readiness through version comparison, audit trails, and streamlined approval workflows.