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5 Reasons to Move to Automated Safety Document Distribution

The very basis of pharmacovigilance is to detect, collect, monitor, and assess reports on adverse events from drug…

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Managing a clinical trial is no small feat. Documents must be tracked, client sites monitored, notes and findings to…

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The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the processes for assessment and supervision of clinical trials…

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Considering switching from a paper trial master file to an electronic one? There’s no better time than now. According to…

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Every person who wants to participate in clinical research should have the opportunity to do so…

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looking at slide under microscope

Managing your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t…

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Advances in clinical trial design and technology are significant contributors to medical progress. However, they also hamper clinical operations and…

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A woman works in a lab

Change is the lone constant you can depend on. When it comes to scientific discovery, most of that change…

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Why Having a Well-Prepared eTMF is Important A well-prepared Electronic Trial Master File (eTMF) is critical to the success of…

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Contract Research Organizations (CROs) have been enthusiastic early adopters of the LifeSphere electronic Trial Master File…

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ArisGlobal Launches LifeSphere NavaX™   Learn More

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