Table of Contents For many research centers or networks, traditional methods such as paper documentation and non-integrated systems have become major bottlenecks, slowing down processes and compromising data accuracy. The Instituto de Investigations Clinicas Mar del Plata in Argentina faced similar challenges but transformed its operations by implementing an electronic source document and a… Continue reading Electronic Medical Records in Clinical Trials
Table of Contents Why are patient recruitment and retention important for clinical trials? A clinical study’s purpose is to answer a research question. To do so, researchers must recruit appropriate participants and retain as many as possible for the period specified in the protocol. If recruitment or retention is insufficient, a study may not… Continue reading Patient Recruitment in Clinical Trials
Table of Contents Despite its critical nature, decision-making in research centers often relies on traditional methods, leading to inefficiencies and errors. This blog discusses how real-time, data-driven decision-making is transforming the clinical research landscape. It highlights the crucial role of dashboards in optimizing operational efficiency, improving patient outcomes, and streamlining the clinical trial execution process.… Continue reading The Power of Data in Clinical Trial Execution Decision Making
Table of Contents Since 2010, regulatory bodies globally have expressed interest or provided written guidance on their expectations regarding the electronic source document (eSource). What is an electronic source document? eSource refers to using electronic systems and devices to capture, collect, and store data during clinical trials. This includes direct data entry by patients, healthcare… Continue reading Why implement electronic source documents (eSource) in clinical research centers?
Cancer is a leading cause of death in Latin America, with the region experiencing an alarming rise in cases. It is projected that by 2040, 9 out of 10 of the most populous nations in Latin America will see an increase of at least 64% in the number of people diagnosed with cancer annually. This… Continue reading Cancer Research in Latin America
New medical treatments haven’t reached everyone equally. Why? A lack of diversity in clinical trials. African Americans make up 13% of the US population but only 5% of clinical trial participants. Similarly, Hispanics are vastly underrepresented, comprising 15% of the population but just 1% of trial participants. (1) This disparity has real-world consequences. Treatments… Continue reading Why Diversity in Clinical Trials Matters
Clinical trial participation is the core of future medical advances. But for sites, recruiting patients in clinical trials and conducting them on the journey is usually a challenging task, driving to nearly 80% of trials failing to meet on-time enrollment (1). In a digital era, technology is at the service of improved trial participation and… Continue reading Six Benefits of Automating the Recruiting Flow in Clinical Trials
Table of Contents What is eConsent and How Does it Improve Clinical Trials? We all recognize the vital role informed consent plays in clinical trials. These trials operate under a complex set of regulations governing how consent is obtained. It is estimated that eConsent implementation in clinical trials reduce the time spent on consent-related tasks… Continue reading eConsent Software for Optimal Clinical Trials
Daily site operations and visit scheduling are often a burden for clinical research teams, who constantly seek to engage and build long-term relationships with participants. Dealing with tight deadlines, extensive planning, and assessments are tasks that impact the point-of-care services and staff workload. A software tool like Trial360, which includes an integrated scheduling system, can… Continue reading Scheduling at Research Sites: From a Problem to an Opportunity
How is the billing of clinical protocols in Trial360? In the world of clinical research studies, a key focus is on precision, compliance with regulations, and maintaining ethical principles. However, effective financial administration is often overlooked. Amidst the complexity of clinical trials and scientific quests, diligent planning, implementation, and recording systems are crucial, piling… Continue reading Clinical Invoicing Software: A Practical Walkthrough with Trial360
