Regulated Temperature Monitoring

Regulated scientific or analytical work in the pharmaceutical, biotech, or food industries often requires that reagents or products be stored in defined environmental conditions. In the pharmaceutical industry, all work that is done under FDA Good Laboratory Practices (GLP) requirements requires that records be kept of the temperatures of storage units.

It is sometimes not necessary to use an automated system, charts and manually recorded temperatures are acceptable to the FDA as long as a written procedures exist, are clear, in place, followed, and are appropriate to the quality of the substance being stored. Records must be stored  according to GLP rules.

If you are using manual methods like a chart or other paper records, you are spending time and money to implement these procedures. Is there a way to get better compliance data at lower cost?

About the Tempurity System and Regulated Temperature Monitoring

The Tempurity System uses your standard computer network to collect temperature and other environmental data from your regulated freezers and incubators. For more about the compliance features of  Tempurity click here.

Whether you are a pharmaceutical or biotech organization subject to GLP regulations, or an FDA-regulated company with HACCP requirements the network-based Tempurity System is right for you. Call Networked Robotics today to move quality and safety to a higher level at your organization.

877 FRZ TEMP ( 877 379 8367)

877 GLP TEMP ( 877 457 8367)

Tempurity will collect data from ALL of your organization's monitored devices, wherever they are in the world. For different perspectives you may wish to read more from specific categories below: