Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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SEARCH JOBSElectronic 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.
Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.
Increase transparency, improve communications and reduce administrative burden for all clinical trial stakeholders.
Ease the burden on your sites and make it easier and more appealing for patients to enroll and remain engaged.
Combine data science, technology, and analytics driven by artificial intelligence to support new efficiencies and business insights -- without additional capital investment.