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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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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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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