Nermin is Global Medical Director at Erbe Elektromedizin, leading clinical evidence strategy, regulatory submissions, and trial design for novel medical devices. A gastroenterologist, Full Professor of Internal Medicine, and author of two medical textbooks, he has published over 80 peer-reviewed papers across two decades.
The required mix of software engineering, regulatory knowledge, and clinical-risk judgment is unusually narrow. Here’s how to close the gap.
By Nermin Salkic
13 min read
A clinical trial data platform is not one system. Here's how engineering leaders decide what to buy, augment, or build, and why getting it wrong costs millions.
By Nermin Salkic
19 min read
AI clinical decision support systems usually fail at the architecture layer. Here’s why clinicians override most alerts, and what working systems get right.
By Nermin Salkic
18 min read