Andres Felipe Pineda Torres 7 Principles for Good Clinical Practices in Clinical Trials Table of Contents Adherence to Good Clinical Practices (GCPs) is mandatory in clinical trials. These rigorous standards ensure safety, ethics, and reliability in medical research. However, GCP complia... Resources Trial 360 Oct 21, 2024
Andres Felipe Pineda Torres Efficiency in Clinical Trials: Excel vs CTMS? Table of Contents Utilizing CTMS can cut operational costs by about 25%, making clinical trials more cost-effective. This significant reduction in expenses allows research centers to allocate resource... Resources Trial 360 Oct 9, 2024
Andres Felipe Pineda Torres Integra IT at Global Site Solutions Summit The Global Site Solutions Summit™ has been committed to being “the site’s meeting.” The Summit provides a unique hub where sites, sponsors, CRO executives, and regulators come together to discuss best... News Sep 27, 2024
Andres Felipe Pineda Torres Electronic Medical Records in Clinical Trials 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 compromis... Resources Study Cases Trial 360 Sep 2, 2024
Andres Felipe Pineda Torres Patient Recruitment 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 p... Resources Trial 360 Aug 27, 2024
Andres Felipe Pineda Torres Phase I Vaccine Trials & ePRO: Ensuring Patient Safety Table of Contents When developing new vaccines, patient safety is paramount. Phase I vaccine trials determine safety and efficacy before public release. Data collection is crucial for evaluating the v... Resources TrialPal Aug 23, 2024
Andres Felipe Pineda Torres The Power of Data in Clinical Trial Execution Decision Making 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-dr... Resources Trial 360 Aug 2, 2024
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 2024 FDA Draft Guidance on Diversity Action Plans: Enhancing Inclusion in Clinical Studies On June 26, 2024, the FDA issued new draft guidance describing the format and content, medical products, clinical studies, timing, and process for submitting diversity action plans. Likewise, the crit... News Jul 11, 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 4 Key Benefits of AI & Machine Learning in Clinical Trials Artificial intelligence (AI) and machine learning (ML) herald a new era of regulatory operations in clinical trials. These advanced technologies are revolutionizing how companies manage regulatory dat... Resources TrialPal Jun 13, 2024
