Remote monitoring of clinical trials in Trial 360: Innovation for a More Efficient and Safe Future Clinical trials are vital in developing and approving new drugs, treatments, and medical devices. The regulation requires monitoring of clinical trials to ensure the accuracy and reliability of the data generated by the trial. Monitoring includes reviewing data and… Continue reading Remote monitoring of clinical trials in Trial 360
Scheduling at research sites is not as straightforward as in other clinical services. Commonly, patient visits must be scheduled according to a research protocol and their compliance is essential for the success of the study. Using an intelligent scheduling system can bring great advantages to the research team, among them: Reduction of protocol deviations Thanks… Continue reading Four Benefits of Having a Smart Scheduling System in Sites
Over the years, migration trends have changed, and the United States still has the highest rates of immigrants globally. This reality has impacted public health and healthcare access, demanding legislation and policies such as providing prenatal care to women regarding their immigrant status, which has been adopted in 18 states (1). On the other hand,… Continue reading Remarks On Engaging The Hispanic Community In Clinical Trials, and how technology is helping
Trial360 delegation log is a vital tool for research sites. It serves several crucial purposes, ensuring compliance, accountability, and efficient study conduct.Get enhanced accountability by clearly assigning tasks and responsibilities, ensuring everyone is aware of their specific roles. This helps identify any potential issues with task execution. Additionally, with a robust Delegation Log, research… Continue reading A Compliant and Easy to Setup Delegation Log with Trial360
Around this season, many research sites are planning and projecting their budget for the upcoming year 2024; this is an excellent opportunity to consider a key investment in technology and data-driven management that will bring efficiencies and savings in the short, medium, and long term. By implementing Trial360, sites can go paperless, as well… Continue reading Are you planning your site’s 2024 budget?
Trial360 new enhanced PI – QA – Data entry Oversight Feature The new and improved quality review functionality within Trial360 seamlessly integrates quality assessments directly into the visit process. Effortlessly capture review details, including date, time, reviewer name and role, responsible party, a description field, and the option to link findings and deviations to the… Continue reading Streamlined Quality Reviews with Trial 360
We chose Odoo business suite (ERP, CRM, etc) as the foundation for Trial 360 because it offers the robustness, security, flexibility, experience, and scalability that every company needs. Clinical Research Centers lack a unique platform to conduct clinical trials, business, and administrative and finance processes. Odoo’s proven track record in other industries and adaptability allowed… Continue reading Why is Trial 360 based on Odoo Business Suite?
Recently, we participated in the global meeting of research centers of the Society for Clinical Research Sites – SCRS in Hollywood – Florida. Today, we want to share with you some topics that we identified and will be important for the clinical research industry for research sites. Participant-centered care: A participant-centered and needs-based approach will… Continue reading Trends and Insights for Research Sites in 2024
At Integra IT we have identified the great opportunity for research sites of beeing visible in the digital environment. The sites can gain competitiveness, recognition and positioning by having a high-quality digital cover letter, that speaks of their value proposition, differentials, experience and that work as the direct contact channel with potential customers, patients… Continue reading Having a Website: Key to Boost Research Sites Success
The Food and Drug Omnibus Reform Act of 2022 (FDORA) was signed into law, amending the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act. It includes provisions that impact various aspects of the FDA-regulated industry. Some key provisions include reauthorizations of FDA programs, reporting requirements for approved biological products, improvements in… Continue reading Implications of The Food and Drug Omnibus Reform Act of 2022 (FDORA) for the clinical trial industry
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