Real-Time Visibility with SteriLink

SteriLink is an online, interactive service that provides complete, real-time visibility into STERIS processing facilities*. The SteriLink service is designed to shorten time between manufacturing and distribution by allowing you to:

  • Monitor your inventory, 24/7
  • Receive alerts
  • Review and retrieve historical processing documents
  • Check performance metrics and generate reports

In short, you gain complete, real-time visibility into our facilities so you can make critical supply chain decisions faster.

See More. Control More.

E-mail alerts keep you informed on where your product is in our contract sterilization process. You’re also able to access supply chain and quality documentation to help shorten your time to market.

Document Retrieval

The document retrieval function lets you access documents directly from SteriLink.

Documents accessible through SteriLink include:

  • Receiving Report
  • Count Discrepancy Report
  • Damage Report
  • Ethylene Oxide Certificate of Processing Report
  • Ethylene Oxide Detailed Run Record Report
  • Gamma Certificate of Processing Report
  • Gamma Run Dose Record Report
  • E-beam Certificate of Processing Report
  • E-beam Run Dose Record Report
  • X-ray Certificate of Processing Report
  • X-ray Run Dose Record Report
  • Shipping Document / Bill of Lading Report

E-mail Alerts

Customers can also receive automatic e-mail notifications as product moves through the process.

SteriLink email alerts include:

  • Product Was Received Alert
  • Product Damage Alert
  • Inventory Count Discrepancy Alert
  • E-beam Certificate of Processing and Dose Report Was Signed Alert
  • E-beam Certificate of Processing Was Signed Alert
  • E-beam Dose Report Was Signed Alert
  • Ethylene Oxide Certificate of Processing Was Signed Alert
  • Gamma Certificate of Processing and Dose Report Was Signed Alert
  • Gamma Certificate of Processing Was Signed Alert
  • Gamma Dose Report Was Signed Alert
  • X-ray Certificate of Processing and Dose Report Was Signed Alert
  • X-ray Certificate of Processing Was Signed Alert
  • X-ray Dose Report Was Signed Alert
  • Product Was Shipped Alert

How to Sign Up for the SteriLink Service

Please go here to register.

The SteriLink application was tested and validated in accordance with regulatory requirements found in FDA regulations 21 CFR Part 211, 21 CFR Part 820, and 21 CFR Part 11.

* Some locations may not have availability at this time.  Please contact us for more information.

Watch our Introduction to SteriLink Supply Chain Visibility video to learn more.