Imagine a world where participating in clinical research is as simple and unobtrusive as a routine check-up. Decentralized Clinical Trials (DCTs) have the potential to do that if they put the patient at the center when planning their trials. In this blog, we’ll unravel how DCTs are not just a …
About The clinical research industry is perpetually evolving, refining processes for optimal outcomes. While traditional feasibility has centered on site and country selection, a pivotal aspect remained overlooked – the patient. Patient Feasibility bridges this gap, offering a holistic approach that combines technology and human experience for comprehensive clinical trial …
The New Generation of Clinical Trials: Powered by Patient Feasibility and AI Read More »
*NB: The images below are clickable for a full size view. In the clinical research industry, AI like ChatGPT and Bard, built on large language models (LLMs), have emerged as tools, used to derive information with efficiency. Yet, data accuracy is not their strongest suit. LLMs have the potential to empower …
ChatGPT’s Limitations in Clinical Research: A Call for Advanced AI Read More »
The clinical research landscape is on the brink of an exhilarating transformation. As we stand at this technological juncture, we proudly introduce TrialHub – not just a tool, but a process that promises to redefine the way we understand clinical trial feasibility. Unlock Fast and Accurate Insights: The need for …
Introducing: The 360-degree Knowledge Hub for Clinical Research Read More »
The clinical research industry has been on an evolutionary journey, continually adapting and refining processes to optimize results. Central to these endeavors has been country and site feasibility—key factors in determining the odds of success of a clinical trial. However, despite the comprehensive nature of these feasibility assessments, one critical …
Patient Feasibility: The Game Changer For Your Clinical Trial Planning Read More »
Underrepresentation in clinical trials presents not just an ethical but also a medical issue. Yet, diverse patient populations can be hard to reach without the data needed to locate them, understand their unmet needs and remove the barriers to participation. TrialHub represents a new way of conducting feasibility, one that …
TrialHub Empowers EmVenio to Identify New Trial Sites and Expand Access to Research Read More »
When planning a clinical trial, selecting the right location is just as crucial as timing your drug’s release. We’ve observed over the years that more than traditional feasibility alone is needed to secure a successful trial. So, what’s the essential component we’re overlooking? Tick-Tock, Watch the Clock: Time is of …
The 3 Reasons Why Traditional Feasibility is Not Enough When Planning Clinical Trials Read More »
ChatGPT has become incredibly popular not just among AI enthusiasts and content creators but also within our clinical research industry. More than the chat bots we are familiar with, ChatGPT does not simply come back with scripted replies. But AI is not God – at least for now it isn’t …
What Makes or Breaks a Clinical Trial According to ChatGPT (A.k.a the Industry) Read More »
Clinical research is a conservative industry – when something new makes its way to the influencers and the KOLs, the big established companies can be quite skeptical. After all, though they may have resources, they also have a lot to risk by investing in a trend that won’t be relevant …
We Tackled Clinical Trials Data Inaccuracy So You Don’t Have To Read More »
Lukasz Wozniak joined the industry in 2005 working for CRO companies. He has been working independently since 2010 as a freelance clinical trial consultant contracted by pharmaceutical and CRO companies covering CRA and regulatory affairs positions. Overall, Lukasz has 16 years of experience in research and in recent years, he …
Clinical Research in Poland: Excellent Recruitment and DCT Adoption Read More »
María López is a freelance clinical research consultant and part of TrialHub’s network of country advisors. She has 25 years of experience in clinical research both in medical devices and drug clinical studies. Over the years she has held different positions: field clinical monitor, clinical research associate, clinical trial manager, …
The Benefits of Conducting a Clinical Trial in Spain Read More »
We help CROs and sponsors to stop fixing patient recruitment challenges and start preventing them.
