Speaking your language - elevate your clinical labeling and content management

In recent years, the clinical trials industry has undergone significant transformation. This new normal has introduced added complexity, evolving regulations, and heightened expectations for faster outcomes. Beneath every label lies the challenge of managing intricate content across multiple countries, language requirements, batch size adjustments, patient/study specific data, and regulatory requirements - factors that can introduce costly unknowns, extend timelines, and increase operational risk.

In this webinar, discover how to proactively meet diverse production, supply, and regulatory demands. Without careful management, labeling can quickly become a significant bottleneck in the clinical trial supply chain, potentially derailing the progress of a study. We will demonstrate how to:
  • Build the study label, check regulatory content based on destination, and print clinical trial labels in minutes
  • Leverage a populated phrase library & reg rules engine to generate multi-page booklet label artworks at speed and show how a late-stage change can be accommodated
  • Ensure compliant labels for everchanging local requirements
  • Generate on-demand language specific labels for small batch & JIT production
  • Simplify global language requirements by reusing content
SPEAKERS

Steve Ellison, Director Clinical Trials, Loftware

Steve has spent over 25 years working with coding and labeling solutions.  His most recent role has been overseeing Clinical Trials Sales for Loftware sharing his knowledge with the clinical supplies industry.  

Hal Green, Senior Solution Architect, Loftware

Hal has over 14 years’ experience as a Solution Architect specializing in Digital Transformation in highly regulated industries such as Oil and Gas and Life Sciences industries. His experience allows him to critically analyze customer processes to ensure the solution is effective and efficient. 
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