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Read MoreSimplifying Patient Visit Scheduling with Cosmos
Simplifying Patient Visit Scheduling with CosmosIn clinical research, one of the most time-consuming challenges for sites is managing patient visit calendars. Between juggling multiple study protocols,[...]
Read MoreCosmos eSource: Smarter, Faster, and Always Audit-Ready
Clinical trials demand precision, speed, and compliance and nothing is more critical than being audit-ready at all times. With growing expectations from sponsors and regulators, sites[...]
Read MoreStreamlining Clinical Trial Operations: Visit Scheduling, eSource, and Compliance Made Easy
Introduction to Clinical Trial EfficiencyClinical trials are becoming increasingly complex, with tight timelines, diverse patient populations, and regulatory requirements. One of the biggest challenges sites face[...]
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Free Clinical Research Training: ICH GCP, HIPAA & IATA Certification🚀
In today’s fast-changing world of clinical research and clinical trials, success depends on knowledge, compliance, and the right tools. That’s why COSMOS Academy, part of the[...]
Read MoreExploring Key Features of COSMOS Clinical eRegulatory (eReg) System
In the evolving landscape of clinical research, regulatory compliance is non-negotiable. Historically, research sites relied on physical binders, paper logs, and manual filing systems to manage[...]
Read MoreHow to Measure eSource ROI: A Practical Framework for Research Sites
As clinical research transitions from paper-based methods to digital-first operations, eSource (electronic source data capture) has emerged as a key driver of efficiency, compliance, and data[...]
Read MoreQA Remote Monitoring & Study Compliance in a Changing World
Leveraging ICH GCP R3 and COSMOS CTMS for Modern Clinical OversightIn today’s evolving clinical research landscape, remote monitoring has transitioned from an optional add-on to a[...]
Read MoreA Checklist for Optimizing Clinical Trial Study Startup Activities
The study startup phase is one of the most critical and complex stages in the clinical trial lifecycle. It sets the tone for the rest of[...]
Read MoreWhy Your Institution Needs an eRegulatory System: A Digital Transformation Aligned with ICH GCP R3 and COSMOS CTMS
As clinical research becomes increasingly complex and globally distributed, institutions must modernize their processes to keep pace with regulatory requirements, streamline workflows, and maintain compliance. One[...]
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