While eConsent has become a reality in the US, Europe is still lagging behind in its implementation. To protect patient rights without compromising on the full potential of clinical research, flexible and dynamic consent formats will be crucial in the future.
Der digitale Fortschritt durchdringt das tägliche Leben in allen Bereichen. Die getroffenen Maßnahmen im Zuge von COVID-19 haben dazu beigetragen, dass diese Entwicklung vor allem im Gesundheitsbereich noch verstärkt wird.
The use of electronic data capture (EDC) and electronic case report forms (eCRF) is becoming the gold standard in clinical research. Today, the dream of a paperless (or at least near-paperless) study seems within reach [...]
To ensure a perfectly suited eCRF design many different aspects have to be taken into account also with regard to user-friendliness [...]
The electronic case report from (eCRF) played a pioneering role in the digitalization and introduction of ever new technologies into clinical research, and enjoys great popularity. Here, we would like to give you a short overview of how an eCRF develops in the course of a study.