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
"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
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
Bottlenecks in clinical trials often start at the source – the way data is captured and entered. Manual data entry processes slow progress and introduce unnecessary risks, including transcription errors,... Read More