A clinical researcher using eConsent in clinical research wearing a white coat sitting at the table.

eConsent in Clinical Research: Evaluating the Regulatory and Ethical Concerns

In recent years, technology has become a fundamental part of clinical research. As advances in software and hardware have made gathering data from participants easier and more efficient, electronic consent (eConsent) in clinical research has become increasingly popular. But what are some regulatory and ethical considerations that researchers should be aware of when implementing eConsent?…

Two individuals conducting medical research involving RTSM in Clinical Research

RTSM in Clinical Research: How Can Medical Researchers Benefit From The Technology

In the world of clinical research, the use of technology is becoming increasingly important to increase accuracy. One technology gaining traction is Randomization and Drug Supply Management (RTSM). RTSM in Clinical Research is a powerful tool that allows medical researchers to gain valuable insight into their research and uncover new opportunities for improving their methods. In…

An ongoing clinical trial

Digital Clinical Trials: Finding Success in a Challenging Regulatory Environment

With the ever-increasing demand for digital clinical trials, the global healthcare industry is faced with a unique challenge―navigating a complex regulatory environment. Continue reading this blog to explore how to conduct successful clinical trials in this rapidly evolving space. Make A Clinical Trial Plan Conducting a clinical trial requires careful planning and execution, especially when navigating…