eSource in clinical trials

Digital Transformation: Harnessing eSource in Clinical Trials

The pharmaceutical industry is undergoing a significant shift towards digital transformation, and clinical trials are no exception. One of the key drivers of this transformation is the adoption of eSource, electronic data capture, and other digital technologies.  This blog will explore the benefits and challenges of harnessing eSource in clinical trials and how it can…

remote monitoring in clinical trial

Remote Monitoring in Clinical Trials: A Comprehensive Overview

Clinical trials are the backbone of medical research, enabling the development of new treatments, medications, and medical devices. However, conducting clinical trials can be a complex, time-consuming, and costly process. Remote monitoring has emerged as a game-changer in clinical trials, revolutionizing the way data is collected, monitored, and managed.  In this blog post, we’ll explore…

remote clinical trial monitoring

Insights into Remote Clinical Trial Monitoring Practices

The clinical trial landscape is undergoing a significant transformation, driven by technological advancements, regulatory changes, and the need for more efficient and patient-centric approaches. Remote monitoring clinical trial practices have emerged as a crucial aspect of this transformation, offering a new paradigm for conducting clinical research.  In this blog, we’ll delve into the insights of…

On-going training program in a conference room.

A Comprehensive Guide to Developing a Clinical Research Training Program Checklist

Training is often considered a prerequisite and one of the essential components of clinical research. With proper training, researchers understand all the ethical implications of the study and stay compliant with all the regulations throughout the study. To that end, the training aims to teach the researchers about all the steps of the research, from…