eConsent clinical research

eConsent: What it is and Why your EDC Software Should Have it

The healthcare industry is not lacking in buzzwords or new tech terminology as of late. eConsent, short for electronic informed consent in clinical research, is one of the terms that seems to be here to stay. According to the Food and Drug Administration (FDA), eConsent refers to the “use of electronic systems and processes that […]

Still Using Paper CRFs in Clinical Trials?

By: Dr. Leigh J. Mack | Chief Medical Officer Does your clinical trial look like this? The year is 2018. A sponsor for a new anti-arrhythmic medication and a CRO meet to discuss the strategy for a Phase 3 national clinical trial on the all-in-one system, Clinical Studio, that integrates other peripheral systems. What would […]