On-demand webinar: new approaches to automating temperature management in clinical trials

A scientist using a tablet in a modern laboratory.
Temperature excursion management is a prime example of a clinical process that automation can make more efficient. It is currently a highly burdensome activity, where every temperature excursion is evaluated regardless of how minor they are and if they fit well within the excursion budget.

Data technology for End-to-End clinical supply management

Further benefits can be realized through integration and new technologies. For example, most clinical sites and sponsors still use USB loggers that require manual uploads by site personnel; data is continuously and automatically captured and available in the cloud through data uploads with IoT technologies. Moreover, by integrating with an IRT solution, any treatments that experience a deviation automatically quarantined, ensuring that they are not dispensed to patients.

Watch this webinar where we discuss how automation can help you transform the temperature management process to create more efficient workflows for all study stakeholders.  

Agenda:

  • Current processes for handling excursions​
  • Removing stakeholder burden while ensuring complete data
  • Automating excursion review and analytics for efficient supply chains​
  • Interoperability between clinical systems​

Speaker 

Evan Hahn

VP North America

TSS 

 

Watch now

Watch now or download it by completing the form below: 

You may also be interested in

A stethoscope resting on documents with overlaid data graphs, representing the Clinical Trial Supply East Coast event.

We are back at Clinical Trial Supply East Coast

We are excited to join the 20th Anniversary edition of Clinical Trial Supply East Coast on the 19th and 20th October 2022 in the Sheraton King of Prussia. The conference covers all things CTS from reducing timelines and streamlining processes to handling clinical supplies in a decentralized trial world. Along speakers from Pfizer, Merck, Janssen and many more we will present how digitalization of temperature processes can improve business outcomes in clinical trials.
Read moreDownload Whitepaper

Can You Rely on the Results from Your Clinical Trials?

The success of a clinical trial depends on the reliability of its data. Many investigational drugs are sensitive to temperature, and any temperature deviation can affect their quality and, in the worst case, patient safety. Automated and integrated temperature monitoring solutions help secure data quality, support compliance, and speed up the delivery of new medicines to patients.
Read moreDownload Whitepaper

Logipharma report: A fast-track learning exercise in pharma supply chain innovation

In Q4 of 2021, WBR Insights surveyed 100 Directors of Supply Chain Management and similar from pharma organizations across Europe and North America to find out about the challenges they face in 2021 and the innovative solutions they are putting in place.
Read moreDownload Whitepaper

You may also be interested in

Can You Rely on the Results from Your Clinical Trials?

The success of a clinical trial depends on the reliability of its data. Many investigational drugs are sensitive to temperature, and any temperature deviation can affect their quality and, in the worst case, patient safety. Automated and integrated temperature monitoring solutions help secure data quality, support compliance, and speed up the delivery of new medicines to patients.
Read more

Extending TempMonitor BLE to Ultra-Low Temperatures

Introducing the new TSS Dry Ice Probes, enginereed for accurate and GxP-compliant temperature monitoring down to –90°C. Available in two lengths for flexible setup — built to safeguard product integrity in every environment.
Read more

Subscribe to our newsletter

Sign up for our newsletter to receive all the latest TSS news and insights in temperature management solutions.