Andres Felipe Pineda Torres Why implement electronic source documents (eSource) in clinical research centers? 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 elect... Resources Trial 360 Jul 15, 2024
Andres Felipe Pineda Torres Cancer Research in Latin America 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 wil... Resources Trial 360 Jun 18, 2024
Andres Felipe Pineda Torres Why Diversity in Clinical Trials Matters 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. Sim... Resources Trial 360 Jun 14, 2024
Andres Felipe Pineda Torres Six Benefits of Automating the Recruiting Flow in Clinical Trials 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... News Trial 360 May 20, 2024
Andres Felipe Pineda Torres eConsent Software for Optimal 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 regul... Resources Trial 360 Apr 30, 2024
Andres Felipe Pineda Torres Scheduling at Research Sites: From a Problem to an Opportunity 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 deadlin... Resources Trial 360 Mar 29, 2024
Andres Felipe Pineda Torres Clinical Invoicing Software: A Practical Walkthrough with Trial360 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. Howeve... Resources Trial 360 Mar 6, 2024
Andres Felipe Pineda Torres Efficiency in execution of research protocols Welcome to the forefront of efficiency in research protocols execution! Protocol research centers struggle with balancing quality and affordability. Trial360 emerges as a beacon of innovation, offerin... Resources Trial 360 Feb 27, 2024
Andres Felipe Pineda Torres How to Ensure Quality Control in Clinical Research? To establish confidence in the results of clinical research, quality control in the execution of the protocol is an essential pillar. Quality control must guarantee the research results' integrity, sa... Resources Trial 360 Feb 23, 2024
Andres Felipe Pineda Torres Findings and Deviations in Trial 360 Clinical research protocols are carried out following the International Council for Harmonization (ICH) guidance on Good Clinical Practice (GCP), which outlines the requirements for corrective and pre... Resources Trial 360 Feb 7, 2024
Andres Felipe Pineda Torres What are the requirements of Audit Trail in CFR 21 Part 11? In the 21 CFR Part 11, the FDA established guidelines for electronic records and electronic signatures. A fundamental aspect of compliance in clinical trials is maintaining a secure and comprehensive ... Resources Trial 360 Feb 6, 2024
Andres Felipe Pineda Torres Remote monitoring of clinical trials in Trial 360 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... Resources Trial 360 Jan 31, 2024
