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QualioDesign Controls Software

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Get your medical device to market faster. Pull your device design data together and stamp out risks. Focus on building a great medical device - without the headache of manual compliance work.

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A smarter way to manage design controls

Challenge

  • Quality teams work in one system. Engineering teams in another.
  • Siloed and disconnected teams and platforms make traceable, compliant product development impossible to manage.
  • Work grinds to a halt, quality and development work against each other, and your path to market becomes a complex nightmare.

Solution

  • Qualio Design Controls offers a single source of truth for all your product development activities.
  • Pull product data into Qualio with integrations. Control inputs, requirements and risks. Bring your quality and engineering teams into sync.
  • All underpinned by a complete, compliant document stack to show your auditors.
Unite systems and data to enable effective collaboration and stop delays
  • Demolish quality and engineering siloes by connecting systems like Jira, Azure DevOps and TestRail to Qualio
  • Build a real-time, always-up-to-date document stack that flows seamlessly from your engineering team to quality 
  • Centralize all design control data by product, from requirements to inputs, outputs, risks and drag-and-drop attachments
Maintain end-to-end traceability across systems in real time
  • Easily pinpoint missing tests, risk mitigations and more for a right-first-time approach
  • Drive changes and product updates quickly and easily
  • Unlock 100% traceability across design elements while your engineering teams work in the source systems they know and love
Generate release documentation with one click
  • Easily produce quality documentation to ensure you’re delivering a safe and effective product, eliminating time-consuming paper-based processes and manual governance
  • Be 100% audit-ready at all times with documentation, e-signatures and objective evidence
  • Access automated snapshots of product documentation for each stage of your product lifecycle
Purpose-built for your quality and product teams

Quality teams
  • For medical device, SaMD and SiMD companies enjoy a single source of truth for design controls and product data.
  • Export automated documentation, embed FMEA and ISO 14971 risk management and unlock complete traceability from input to output.
Product teams
  • Enjoy uninterrupted development as the engineering systems they`re used to are linked directly to Qualio.
  • Develop and innovate, safe in the knowledge that your work is flowing accurately and in real time straight to the quality department.