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eCRF Data Entry Delays: A Compliance Risk Frequently Underestimated
There is a scenario that everyone working in clinical research knows well. The site is under pressure, priorities keep shifting, and the electronic Case Report Form — which should reflect the real-time status of the study — stops being updated. The data exists: it is in the source documents, often correctly recorded. But it does…
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FDA vs EU: how to keep up with confusing regulations
Future is now. What we used to imagine as something for the year 3000 is already here, woven into our everyday life. Technology has reshaped our habits so profoundly that it’s hard to remember how things worked before. In clinical research, this transformation has been nothing short of pivotal. From Artificial Intelligence (AI) to Software…
