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Mastering the translation of clinical trial labels

Without careful management, labeling can quickly become a significant bottleneck in the clinical trial supply chain, with any delays potentially derailing the progress of a study. 

One of the most complex and lengthiest aspects of clinical trial labeling is efficiently managing the wide array of country-specific labels that are required for a multi-national trial, ensuring that all the label information is correctly translated and that the design and other label elements comply with the relevant local regulations. Without the use of integrated systems, this activity is incredibly labor-intensive, and as trials get more complex and geographically diverse, it gets exponentially harder. 

Consequently, it is not uncommon for booklet label creation, approval, and printing to take many months. However, with a general industry emphasis on speed of delivery this timeline simply does not work. 

In this webinar, we will investigate how sponsors and their outsourcing partners in clinical supplies can find efficiencies in trial processes and the supply chain, by using software automation and streamlined workflows to deliver impactful results.

Key Learning Objectives

  • Understand how to keep full control of label content, approvals, and on-demand printing that allows you to run trials with agility and speed.
  • Discover how to manage single panel and multi-page booklets destined for multiple countries, in multiple languages and conform to multiple regulations.
  • Determine what must be included in a software-based labeling solution to manage language and content requirements compliantly.

Learn how to make impactful changes to your supply chain by reducing timelines from 16 weeks to a matter of days.

  • Cloud
  • Regulatory
  • Supply Chain
  • Clinical Trials

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