Cómo los ePRO están transformando la adherencia del paciente en ensayos clínicos La adherencia del paciente es uno de los grandes retos de cualquier ensayo clínico. No importa lo riguroso que sea el protocolo o lo bien diseñado que esté el estudio: si los pacientes abandonan, los resultados se resienten. Y en muchos casos, la causa no es médica, sino

By Xolomon – Making research accessible When it comes to clinical trials, pharmacovigilance software plays a crucial, yet often underestimated, role. While most attention tends to focus on recruitment, data capture, or monitoring tools, safety oversight is just as critical to the success and integrity of any study. So, what exactly makes a pharmacovigilance system effective, and how can research

Implementing an electronic Case Report Form (eCRF) system is a pivotal step in modernising clinical trial operations. But no matter how powerful your eCRF platform is, its success depends largely on the people using it. For sponsors and CROs alike, team training is not a box-ticking exercise, it’s the key to data quality, compliance, and trial efficiency. Why training matters

In clinical trials, patient safety isn’t just a regulatory checkbox; it’s the backbone of every protocol. Whether you’re running a single-site study or coordinating a multi-country trial, tracking adverse events and unexpected reactions with precision is critical. Pharmacovigilance teams rely on consistent, complete, and timely data to detect safety signals. But too often, safety reporting is siloed from core trial