Soghat JavedWhen 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
A top pharmaceutical sponsor approached us when their global Phase III oncology trial faced significant recruitment delays and compliance issues. The trial spanned 10 countries and required over 500 patients, but fragmented site management threatened the timeline. Here’s how we stepped in to deliver results. The Challenge The sponsor faced these critical hurdles: These challenges … Read more
Selecting the right clinical trial sites is one of the most difficult steps for sponsors. The wrong choice can result in inefficiencies, delays, and compromised data integrity, which ultimately impact both the trial’s success and a sponsor’s reputation. So, it’s pretty necessary to know about what to avoid while selecting clinical trial sites To make … Read more
In clinical research, therapeutic area expertise is an increasingly critical factor when selecting the right trial sites. For sponsors in the pharmaceutical and clinical research fields, choosing the best site with relevant therapeutic expertise offers distinct advantages, from improved patient recruitment to greater compliance with protocol requirements. This article examines the importance of therapeutic area … Read more
Selecting the right site for a clinical trial is crucial to the study’s success. A well-chosen site can ensure smooth recruitment, high retention rates, and reliable data, while a poorly selected site can lead to costly delays and issues with regulatory compliance. Here’s a comprehensive guide on how to choose the best site for your … Read more
A Principal Investigator (PI) is the cornerstone of any clinical trial or research study. Responsible for overseeing the study’s conduct, the PI ensures that the clinical trial is performed with integrity, adheres to regulatory requirements, and prioritizes patient safety. Without a dedicated and qualified Principal Investigator, a clinical trial would face difficulties in meeting compliance, … 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
Site Management Organizations (SMOs) and Contract Research Organizations (CROs) Site Management Organizations (SMOs) and Contract Research Organizations (CROs) are pivotal players in clinical research. Despite their importance, they serve different roles, each contributing their own expertise and resources. Sponsors who wish to improve their clinical trials must understand these differences between SMO vs CRO. This … Read more
How To Start a Clinical Research Study In an Efficient Way Starting a clinical research study seems like a challenge. It’s a process filled with regulatory requirements, intricate study designs, and precise data management. However, with the right guidance and support, you can transform this daunting task into a streamlined, efficient journey. But here lies … Read more
