Clinical Blogs

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

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

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

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

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

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

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

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

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

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