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[...]
Read MoreThe 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 MoreAs 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[...]
Read MoreDiscover how Cosmos CTMS helps research sites stay organized and compliant with real-time tracking, easy templates, and audit-ready tools.In the world of clinical research, regulatory compliance[...]
Read MoreAs academic medical centers (AMCs) continue to manage increasingly complex clinical trial portfolios, regulatory compliance remains a cornerstone of operational excellence and sponsor trust. With growing[...]
Read MoreManaging a clinical trial site often means switching between multiple different platforms, CTMS, eSource, EDC, lab portals, payments, EMRs, and even travel bookings. This fragmentation creates[...]
Read MoreIntroductionClinical research is at a pivotal moment. Traditional paper-based research processes, once the backbone of clinical trials, are now being replaced by intelligent digital systems that[...]
Read MoreIntroductionClinical trials are evolving rapidly, and one of the most impactful innovations reshaping the landscape is eSource—electronic source data capture. Moving beyond traditional paper-based methods, eSource[...]
Read MoreManaging clinical trial participant payments has traditionally been a time-consuming and error-prone process. Delayed reimbursements, manual tracking, and inefficient communication can impact both site performance and[...]
Read MoreThe world of clinical research is on the cusp of a significant transformation with the impending release of ICH GCP R3. This updated guideline isn't just[...]
Read MoreWe are entering a new era in clinical research—an era driven by artificial intelligence, digital systems, and regulatory modernization. With the adoption of ICH GCP E6(R3)[...]
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