When a leading multi-specialty site struggled with delayed recruitment and inefficient workflows for a critical Phase II diabetes trial, they faced mounting pressure to meet deadlines. That’s when they partnered with our SMO. This is the story of how streamlined site support turned things around. The Challenge The site encountered several challenges: These challenges risked … Read more
What is an IRB? (Local IRB Vs Central IRB) Clinical research is a cornerstone of medical advancements, but it comes with ethical and safety concerns that must be rigorously addressed. This is where an Institutional Review Board (IRB) steps in. An IRB is a committee responsible for reviewing and overseeing research involving human participants to … Read more
Inclusion and Exclusion Criteria in a Clinical Trial In 2024 Imagine you’re about to participate in a clinical trial, one that could potentially change the idea of medicine but there lies a critical set of guidelines known as inclusion and exclusion criteria in a Clinical trial. These criteria are like the gatekeepers of clinical trial … Read more
Being a sponsor, managing clinical trials can be a daunting task, which requires careful coordination and expertise. This is where you need an SMO. In order to ensure that clinical trials run smoothly, efficiently, and in compliance with regulatory standards, Sponsor needs SMOs. SMO provides a bridge between sponsors, research sites, and patients, they are … Read more
Patient Recruitment Patient recruitment is a critical aspect of clinical trials, yet it can be one of the most challenging. Without an adequate number of participants, a clinical trial may not be able to produce meaningful results. In this blog post, we’ll explore the concept of patient recruitment, including its importance, strategies for improvement, and … Read more
