DocuLiv
electronic instructions for use
A certified platform for electronic Instructions for Use (eIFU) for medical device manufacturers. EU MDR compliant, always up-to-date.
ISO 27001
certified
EU MDR
compliant
24/7
availability
20 years
of enterprise experience
DocuLIV
when it makes sense
Regulatory pressure is increasing
EU regulation on electronic instructions for use (eIFU) tightens requirements for medical device manufacturers.
Printed manuals cost time and money
Printing, packaging, distribution, updates. Every specification change means new costs and paper waste.
Versions are out of control
Customers work with outdated manuals, complaints are rising, there's no audit trail.
Customers expect digital access
QR code on the packaging, current document online. Not searching through drawers.
What DocuLIV can do
under one roof
Regulatory compliance
Full compliance with EU MDR requirements for electronic IFU. Audit trail, version control, access logging.
Document management
Upload, version, translate, publish. Workflow for review and approval built in.
Customer portal
Public access via QR code or product search. Always the latest version, always available.
Analytics & reporting
Who accessed what, when, which version. Complete audit trail for regulatory authorities.
Multi-language support
Documents in any language. Automatic version management per language. EU MDR compliant across all markets.
API integration
Connect DocuLIV to your product management system. Automatic publication of new documents and versions.
Jak DocuLIV
funguje
DocuLIV is a cloud-based system for managing digital instructions for use (eIFU) and technical documentation. We developed it for medical device manufacturers who need to meet EU regulatory requirements, but it's suitable for any manufacturer looking to digitalize product documentation. Secure, scalable, with API for automation. Built on Symfony, operated on high-availability infrastructure in compliance with ISO 27001.
How it works
under the hood
Document upload & versioning
Upload PDFs, manage versions, track changes. Approval workflow built in.
Public access portal
Patients and professionals access documents via QR code or product search. Always the latest version.
QR code access
Generate QR codes for each product. Scan to access the latest IFU instantly.
Analytics & audit
The manufacturer enters product information alongside production data. The system links data with documentation and generates packaging label materials. The customer downloads current documentation directly from the product page.
Why medical device companies choose DocuLIV
we take responsibility
We operate DocuLIV long-term with ISO 27001 certification. 24/7 availability, guaranteed compliance, audit-ready at all times.
EU MDR compliance
Full regulatory compliance. Audit trail, version control, access logging. Ready for any inspection.
24/7 availability
Patients need access to IFU at any time. High availability on Kubernetes infrastructure.
Instant updates
New document version? Published instantly. No printing, no distribution delays.
One partner for the full lifecycle
Eliminate printing and distribution costs. Savings from day one, compounding over time.
We can do more,
see for yourself
Regulatory compliance from day one
Need more than eIFU? Custom systems for medical device manufacturers.
Custom development
From audit through deployment to long-term operations. We know your system, we respond to regulatory changes.
Security
B2B portal for distribution partners with document access.
One partner for the full lifecycle
From audit through deployment to long-term operations and growth. We know your system, we respond to regulatory changes. Twenty years of experience speaks for itself.
We can do more,
see for yourself
Frequently asked questions
Yes. DocuLIV is designed from the ground up for EU MDR compliance. Full audit trail and version control.
Via QR code on the product packaging or through the online search portal. No registration required.
Yes. Colors, fonts, layout, number of results, sections — everything is configurable via a JSON object. The widget runs in Shadow DOM, so it won't affect your website's styles.
High-availability Kubernetes infrastructure. 24/7 monitoring, automatic failover, 99.9% uptime SLA.
Yes. We handle bulk import of existing PDF documents with metadata mapping.
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