Smart Packaging In Clinical Trials: What Clinical Supply Teams Need To Know

Source: Thermo Fisher Scientific

The adoption of new technologies to accurately and reliably measure patient adherence to trial dosing protocols continues to grow. As clinical teams seek ways to incorporate these new digital tools, there will be an increasing need for members of the clinical supply organization to help facilitate the selection, sourcing, and implementation of the most appropriate technology for a given clinical trial based on the unique needs of a trial’s research protocol design.

The webinar is a mix of a short didactic presentation and a panel discussion with clinical supply innovators from across the industry who have shared their experience and lessons learned as they work to normalize the use of adherence measurement tools and smart medicine packages.

This presentation is Part 2 of our series discussing the role of smart packaging in clinical trials. Our initial presentation on the power of adherence data can be found here: Smart Packaging In Clinical Trials: The Power Of Adherence Data.

Key Learning Objectives:

  • Review the two components of any adherence measurement solution (the measurement solution and the data base platform) and review some of the key features and benefits found in the market today and near future
  • Understand the trade-off analysis that can be used to determine the most appropriate adherence measurement solution
  • Appreciate the key differences in workflows when implementing a trial using smart packaging versus standard packaging
  • Dealing with barriers to change management specific to adoption of new technologies
  • Gain connections and listen to lessons learned shared by industry peers
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