drug safety analytics – Clinical Research Made Simple

Automated Adverse Event Detection in Rare Disease Studies

August 22, 2025

Automated Adverse Event Detection in Rare Disease Studies Enhancing Rare Disease Trial Safety with Automated Adverse Event Detection The Critical Role of Safety Monitoring in Rare Disease Trials Rare disease clinical trials face unique safety challenges due to limited patient populations, heterogeneous disease progression, and the frequent use of novel therapies. Detecting adverse events (AEs)…

Data & Technology, Rare and Orphan Disease Trials

Using EHRs for Real-World Safety Signal Detection in Pharmacovigilance

July 25, 2025

digi

Using EHRs for Real-World Safety Signal Detection in Pharmacovigilance How to Use EHRs for Safety Signal Detection in Real-World Settings Electronic Health Records (EHRs) offer a powerful avenue for monitoring drug safety in real-world settings. Beyond their role in patient care documentation, EHRs are increasingly being utilized by pharma and clinical research teams for early…

Real-World Evidence (RWE) and Observational Studies, Use of Electronic Health Records (EHRs)