by Patricio Ledesma | Mar 5, 2025 | RWE/RWD EDC
In the realm of clinical research, Real-World Evidence (RWE) studies have become an essential component in shaping healthcare decisions and improving patient outcomes. RWE studies utilize real-world data (RWD) collected from sources like electronic health records,...
by Patricio Ledesma | Mar 5, 2025 | Academic Research EDC
Multi-institutional academic studies are critical for advancing scientific research, as they bring together diverse expertise, resources, and perspectives across various institutions.However, managing and coordinating data from multiple institutions can be a daunting...
by Patricio Ledesma | Feb 26, 2025 | EDC Regulatory Standards
In clinical trials, the accuracy and integrity of data are paramount to ensuring the safety and efficacy of new medical treatments.Regulatory bodies, particularly the U.S. Food and Drug Administration (FDA), impose stringent standards to safeguard this data, and one...
by Patricio Ledesma | Feb 12, 2025 | EDC Costs
In the world of clinical trials, data management plays a critical role in ensuring the accuracy, integrity, and efficiency of the study process.With the rising costs of clinical trials, especially in smaller-scale studies, managing expenses becomes a priority without...
by Patricio Ledesma | Feb 12, 2025 | Clinical Trials EDC
In the fast-evolving world of clinical trials, data accuracy, speed, and security are critical factors for successful research and development. Electronic Data Capture (EDC) systems have emerged as a cornerstone of modern clinical trials, fundamentally changing the...
