Audit-Ready, Error-Free: Your Guide to Smarter Site Operations

[kc_row use_container="yes" _id="611270"][kc_column width="100%" _id="282698"][kc_single_image image_size="full" _id="225934" image_source="media_library" image="3556" css_custom="{`kc-css`:{}}"][kc_column_text _id="923295"]As clinical trials grow in complexity, site teams face mounting pressure to maintain speed, accuracy, and[...]

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Achieving 30% Faster Operations & 100% Audit Readiness with COSMOS CTMS

[caption id="attachment_3524" align="aligncenter" width="150"] COSMOS CTMS[/caption] In today’s fast-paced clinical research environment, efficiency and compliance are non-negotiable. Research sites require systems that can keep pace with[...]

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Simplifying 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,[...]

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Cosmos 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[...]

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Streamlining 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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Exploring 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[...]

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How 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[...]

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QA 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[...]

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A 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[...]

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Why 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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