eTMF
Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.
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Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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The Electronic Trial Master File: Study Item and Placeholder Analysis
Automated ways to create accurate studies reflective of trial designs
May 31, 2021
Electronic trial master file (eTMF) systems are proving to be effective in maintaining inspection-readiness and compliance.
This paper explores planning wizards and placeholder creation for different types of expected study items and how automation can streamline eTMF management, enabling greater transparency and easier navigation.
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