A clinical trial management system (CTMS) is a software that centralizes and organizes all aspects of clinical trials. It enables sponsors, CROs, and research sites to track participants, manage sites,... Read More
Author: shirleyclinion
"Multi-Agentic AI in clinical trials is a coordinated network of specialized AI agents that think, decide, and adapt together. Acting like a self-orchestrating research team, they accelerate study design, monitoring,... Read More
"Multi-Agentic AI in clinical trials is a coordinated network of specialized AI agents that think, decide, and adapt together. Acting like a self-orchestrating research team, they accelerate study design, monitoring,... Read More
"Clinion’s Multi-Agentic AI can reduce a Data Manager's workload by 90%, accelerate review cycles, and set a new benchmark for clinical data management efficiency. Despite advances in automation, the daily workload... Read More
A clinical trial protocol is the foundation of clinical research, detailing objectives, study design, eligibility, safety oversight, and data analysis. Its structure ensures consistency and credibility, guiding investigators while protecting... Read More
"Clinion's eTMF software offers a user-friendly platform to manage all your clinical trial documents. Get started fast, maintain control, and guarantee compliance with features like: Rapid deployment (weeks!) Intuitive interface based on... Read More
A clinical study report (CSR) is the most critical document produced from a clinical trial, providing regulators and stakeholders with a comprehensive, unbiased account of the study’s design, methodology, results,... Read More