Welcome to Kerlo Blogs, your go-to destination for valuable insights and updates in the field of clinical research.
As a leading clinical research site management organization, Kerlo Research is committed to sharing knowledge, expertise, and discoveries with the global community.
In our blog section, we delve into a wide range of topics relevant to clinical research sites, including emerging technologies, breakthrough treatments, regulatory updates, and best practices.
So, whether you’re a sponsor, a clinical research site, or simply a patient that is curious about the world of medical research, our blogs aim to inform and educate.
Thank you for visiting Kerlo Research Blogs—Stay tuned for regular updates, expert perspectives, and engaging content.
10 Best Practices for Site Management in Clinical Research
You know what successful clinical trials depend on? They depend on effective site management! Site management in clinical research ensures efficiency, regulatory compliance, and optimal patient outcomes. Managing a clinical research site proficiently is important for preventing violations, maintaining data integrity, and improving trial outcomes. With increasing regulatory demands and technological advancements, sites must adopt … Read more
How Kerlo Research Support Improved Patient Recruitment by 45% in Just 8 Weeks
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
How Our SMO Cut Trial Delays by 35% for a Global Phase III Oncology Study
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
5 Red Flags to Avoid When Selecting Clinical Trial Sites
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
Importance of Therapeutic Area in Site Selection
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
How to Choose the Best Site for Your Clinical Trial In 2024
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
What is a Principal Investigator?
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)
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
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
SMO Vs CRO: Comparing SMO and CRO
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
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
Benefits of a Site Management Organization
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
Top 10 Best Site Management Organizations in the US
Clinical trials are highly complex and require expertise, and a steadfast commitment. This is where Site Management Organizations (SMOs) come into play. SMOs are pivotal in ensuring that clinical trials run smoothly, adhering to strict regulatory guidelines, and ultimately bringing innovative treatments to market. In the US, a few standout organizations have set the benchmark … Read more
What is Patient Recruitment?
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
Types of Clinical Trials – [A Comprehensive Guide]
It is clinical trials that advance healthcare, serving as pivotal gateways to innovation. In addition to driving innovation, these meticulously designed studies also offer the chance to improve treatment outcomes. We’ll dive deep in the diverse landscape of clinical trials as we set out on this journey, shedding light on different types of clinical trials … Read more
What are Clinical Trials? A Detailed Guide
Clinical trials are designed to determine if a new drug or treatment will work on a disease or will potentially be of benefit to patients. Throughout this guide, we will explore how do clinical trials work; clinical trials’ complexities, answer key questions, provide data-driven insights, and examine their profound impact on healthcare. To streamline all … Read more
What Is An SMO? – An Easy Guide In 2024
What is a Site Management Organization? When you talk about clinical research, various entities play crucial roles in ensuring the smooth and efficient execution of clinical trials. One such entity gaining limelight is the Site Management Organization, commonly known as SMO. Did you just skip for a bit while hearing the word SMO? Let us … Read more
