According to governmental data, there are over 400,000 clinical trials taking place in the US currently. A vast majority of these trials are now moving to electronic data capture (EDC) software that allows practitioners and researchers to improve their data management, accelerate the process, and leverage modern clinical research approaches. However, despite the vast popularity of…
Setting up studies and ensuring their seamless operation is a difficult task. It is a multi-faceted process that can be prone to unnecessary delays. There are a lot of stakeholders and decisions involved in setting up study sites. The process can be overwhelming for sponsors, CROs, research sites, and clinicians and has historically been marred…
Clinical research studies hold a very important place in the American patient care sector. From drug trials to diagnostics and interventions, clinic researchers help stakeholders optimize and improve their medical practices to ensure a better healthcare infrastructure is created for the masses. But starting a clinical research study is not an easy task. From acquiring Institutional…
From compliance to budget to tight deadlines, clinical research and trials are often surrounded by an array of challenges. Therefore, in recent years, many pharmaceuticals and medical researchers have started to adopt electronic data capture systems (EDC) to help them better collect, manage, and analyze data. If you’re a clinical researcher or a pharmaceutical company…
Modern research trials are expensive to conduct. CROs, sponsors, clinicians, and everyone involved in clinical trials require a lot of resources to conduct swift, seamless, and result-oriented trials. Therefore, replication is a fundamental concept in modern research trials. To ensure the credibility of any scientific claim or research results, it is essential to replicate the study using…
Clinical trials are integral to the research and development for discovering new treatments and cures. As technology advances, so does the ability to manage clinical trials more efficiently. One such way is through eCRF (electronic Case Report Forms). In this blog, we’ll discuss eCRF and how it can help streamline the clinical trial process. What…
Data privacy is an increasingly important concern in clinical trials, and it’s essential to ensure that patient data is secure. With rising cybersecurity threats, you must be equipped to protect your clinical trial data. In this comprehensive guide, we’ll discuss the latest strategies for ensuring data privacy in clinical trials. Read on to discover how…
Clinical trials are vital for advancing medical research and healthcare, but they often require time and resources. From recruiting participants to monitoring outcomes, a successful clinical trial comprises many steps. In recent years, there has been a growing interest in decentralized trials as an alternative to traditional clinical trials. But what exactly is a decentralized…
Are you finding it challenging to keep up with research staff shortages and the demands of clinical trials? You’re not alone. Many organizations feel the strain of limited staff and resources, especially when running a successful clinical trial. Fortunately, Electronic Data Capture (EDC) optimization can provide a solution. Let’s explore how EDC optimization can help…
Clinical trials are an essential part of the development process for new drugs and treatments, and Electronic Data Capture (EDC) systems are often used to help researchers collect, store, and analyze the data. When designing an EDC system for a clinical trial, it’s essential to keep the end user in mind to ensure the system…