Healthcare

Comply with critical healthcare labeling regulations with TEKLYNX barcode label design software solutions.

Are Your Labels UDI-Compliant?

The FDA has issued a final rule that requires that all medical devices distributed in the United States be labeled with a Unique Device Identifier (UDI). As of September 24, 2016, Class III devices are required to bear a UDI as a permanent marking on the device itself if the device is intended to be used more than once and intended to be reprocessed before each use.

Visit our UDI Labeling Software Solutions page to view more resources, including relevant client success stories, on-demand webinars, and eBooks.

Find out how TEKLYNX fits with your industry:

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TEKLYNX CENTRAL CFR has been leveraged from a solid application platform and wrapped with functionality to provide seamless integration into the entire regulated enterprise. Pharmaceutical companies, high-volume laboratories and other organizations that require a robust Quality Management System will find that Validation of this new product in their end-user environment is extremely straight forward.
- Tony Raymond,Consultant/President of New Harbor SQA