Life Sciences

TEKLYNX can help you achieve compliance with federal requirements for Electronic Signatures and Tracking.

TEKLYNX understands that Life Sciences organizations are facing unique federal regulations around their labeling processes. We are committed to helping these organizations achieve compliance. Our enterprise solution designed specifically to help Life Sciences companies comply with 21 Code of Federal Regulations (CFR) Part 11 seamlessly integrates into the entire regulated enterprise and is extremely configurable.

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


  • Medicine and drug labeling
  • Drug component identification
  • Food & Drug Administration (FDA) 21 CFR Part 11 compliance
  • Lab sample tracking
  • Medical device identification