Medical Device labeling software

Kallik delivers speed to market, compliance and change management for complex product labeling and artwork portfolios that significantly challenge medical device organizations.  Whether driven by localized market requirements, merger and acquisition or the launch of a new product, our software can ensure that your organization completes artwork and labeling projects with unrivalled speed and compliance. 

 

Designed for medical devices

We have over 20 years of experience helping global medical device manufacturers revolutionize their labeling and artwork processes. Our cloud-based, end-to-end labeling and artwork management software, Veraciti™, continually evolves to meet the changing needs of the industry. 

With advanced automation, approval, and artwork generation tools, our software ensures total regulatory compliance, enables a faster speed to market, and provides global scalability and standardization for medical device companies.

 

Ensure labeling compliance

Digitize all of your labeling assets in one cloud-based system, with full audit logs and inbuilt approval processes. With Kallik Veraciti, you can have a single source of truth for all of your product labeling assets, giving you full visibility and the ability to change assets across thousands of labels in seconds. 

With fully customizable role-based digital approval flows, label automation, advanced reporting, and full audit logs, you can ensure total regulatory confidence in your medical device product labeling and artwork. 

End-to-end medical device labeling software


Kallik has a wealth of experience working with medical device organizations and manufacturers. Our label and artwork management solution, Veraciti™ is continuously adapting to the changing requirements of the medical device industry.  Get in touch today and see how Kallik can benefit your labeling and artwork management process.
 

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Medical device labeling software
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Approvals

Ensure Compliance

Simplified EU MDR & IVDR, FDA UDI, FDA 21 CFR 820, FDA 21 CFR Part 11 and EU GMP Annex 11 compliance

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Global

Standardize Global Operations

Support business expansion with quick and easy onboarding of new manufacturing sites via cloud-based labeling software

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quick response

Go to Market Faster

Digitize and streamline your labeling process, allowing you to make changes and approve labels faster and go to market sooner 

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Integrate your systems

Integrate Your Systems

Easy integration with other enterprise systems such as PLM and ERP giving you a single source of truth all in one end-to-end platform

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Full audit trails & logs

Ensure Traceability

Complete traceability and transparency across the medical device supply chain with detailed audit trails of all activity

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Automated artwork creation

Automate Your Processes

Reduce the risk of human errors, ensure compliance and increase efficiency with automated artwork and rules-based decisions

Ossur

 

Össur Case Study

How Kallik helped transform Össur's medical device labeling

 

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