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Book a Personalized qmsWrapper Demo

See how qmsWrapper helps MedTech teams manage quality events, traceability, risk management, document control, CAPA, and FDA/ISO compliance in one connected system.

  • Live walkthrough of relevant workflows
  • Answers tailored to your device and regulatory needs
  • Discussion of implementation approach
  • Pricing and licensing options

No generic sales presentation. Focus on the topics that matter to your team.

Schedule Your Personalized qmsWrapper Demo

See how a Medical Device QMS works in real regulatory scenarios.

What Happens Next?

Submit your request

Complete the form and tell us a little about your company and goals.

Check your inbox

We’ll send you an email with a link to schedule a convenient meeting time.

Meet with our team

See relevant workflows, ask questions, and explore how qmsWrapper fits your needs.

Scheduling emails are usually delivered within a few minutes. If you don’t receive one, please check your spam folder or contact us at contact@qmswrapper.com

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See Your Quality System in One Place

Design Control Software for Medical Devices: Laptop screen displaying the qmsWrapper Traceability Matrix with linked use cases, requirements, risk levels, risk mitigation, and test records in a live, connected DHF view.

What Teams Want to Know Before Exploring a QMS Software Demo

How long does a qmsWrapper demo take?

Most demonstrations focus on the topics most relevant to your team and typically take around 20–30 minutes. We reserve up to 45 minutes in the calendar to allow time for questions, discussions, and specific workflow reviews when needed.

What will I see during the demo?

The demo is tailored to your needs. Depending on your priorities, we can show document control, CAPA, risk management, change control, Technical File management, design controls, traceability, audit workflows, or AI-powered change impact analysis.

How does qmsWrapper support FDA QMSR and ISO 13485?

qmsWrapper supports connected quality workflows, traceability, risk management, CAPA, document control, electronic signatures, and audit-ready records aligned with FDA QMSR, ISO 13485, MDR, IVDR, and 21 CFR Part 11 requirements.

Can qmsWrapper replace spreadsheets and disconnected systems?

Yes. Many MedTech companies use qmsWrapper to replace spreadsheets, paper records, SharePoint repositories, and disconnected quality tools with a single connected quality management system.

How does qmsWrapper handle traceability?

qmsWrapper connects requirements, risks, design inputs, design outputs, tests, quality events, CAPAs, and change controls in a single traceable ecosystem. This helps teams understand how changes affect related records before implementation.

What does qmsWrapper cost?

qmsWrapper uses a simple licensing model with all core modules included. Pricing depends on company size. We can discuss specific pricing during the demo.

How quickly can qmsWrapper be implemented?

Most organizations can begin using qmsWrapper within weeks. The platform is pre-configured for regulated MedTech workflows, reducing the need for lengthy implementation or customization projects.

What makes qmsWrapper different from traditional QMS software?

Unlike traditional QMS platforms that focus primarily on document management, qmsWrapper connects quality events, risk management, CAPA, change control, traceability, and Technical File activities in one system. AI-assisted capabilities help teams understand change impact, maintain traceability, and reduce manual administrative work.