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Maximizing Budgets in Clinical Trials: The Financial Advantages of an Integrated eClinical Solution  

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RealTime eClinical Solutions - Maximizing Budgets in Clinical Trials: The Financial Advantages of an Integrated eClinical Solution

In an analysis published by Nature, nearly a quarter of all trials experienced setbacks due to strategic issues, commercial barriers, and operational challenges. The financial repercussions of such setbacks are significant, with drug developers facing potential losses ranging from $600,000 to $8 million per day. This statistic underscores the critical importance of effective, end-to-end clinical … Read more

Decoding How Sponsors Evaluate Research Sites for Clinical Trials

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Decoding How Sponsors Evaluate Research Sites for Clinical Trials

When selecting clinical research sites for their trials, sponsors look for a blend of capabilities, resources, and a proven track record that promises the best outcomes for their studies. With sponsors seeking top-performing sites that align with their trial objectives, the ability to showcase expertise, efficiency, and reliability is key component of successful to success. … Read more

The Benefits of eRegulatory for Academic Medical Centers 

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The Benefits of eRegulatory for Academic Medical Centers

As of March 2024, there are almost 150,000 clinical studies registered in the United States, with Academic Medical Centers (AMCs) overseeing a staggering volume of clinical trials annually across various therapeutic areas. At the forefront of medical innovation, patient care, and medical education, AMCs drive advancements in healthcare while nurturing the next generation of medical professionals.

What is a Clinical Trial Management System (CTMS)?

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What is a Clinical Trial Management System (CTMS) ?

Clinical trials are fundamental in advancing medical science, offering new treatments and drugs to improve patient care. However, managing these trials is a complex task involving multiple stages and stakeholders. To streamline this process, Clinical Trial Management Systems (CTMS) have become essential for clinical research sites to organize efficient site management.

What is eSource in Clinical Trials? Beyond Paper. 

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What is eSource in clinical trials

Technological advancements and adoption in clinical trials continue to reshape the way data is collected, managed, and analyzed by clinical research sites, sponsors and CROs. Over the last decade, Electronic Source (eSource) has gained prominence for enabling direct data entry by investigators, reducing transcription errors and enhancing data quality.  However, eSource in clinical trials is … Read more

On-Demand Webinar: Mastering FDA Audit Readiness & Easing Site Burden

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Mastering FDA Audit Preparedness

https://vimeo.com/898629213?share=copy Webinar Date: October 25, 2023 Discover the keys to audit readiness in webinar, “Mastering FDA Audit Preparedness: Streamlining Compliance and Easing Site Burden.” Our panel of experts unpack the potential of eRegulatory solutions in solving common compliance challenges. Check out valuable insights that will help you proactively manage FDA audits and compliance requirements.   What … Read more

Events

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Upcoming Events SLEEP Annual Meeting June 14-17, 2026 | Baltimore, MD Details The 40th annual meeting of the Associated Professional Sleep Societies (APSS) brings together the world’s leading experts offering unparalleled opportunities for knowledge sharing, networking, and discovering advances in clinical sleep medicine, sleep and circadian research, and sleep health. Event Website SCRS Australia & New Zealand … Read more

Expedite Your Study Startup – A Site Checklist

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Study startup and site activation are key to the clinical trial process, but often suffer from delays. It can be a time-consuming undertaking and requires multiple teams and moving parts to successfully begin a trial at the best sites for the protocol. In fact, a recent ACRP survey revealed that study startup was ranked among … Read more

Accelerate Study Cycle Times with Clinical Trial Software for CROs

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In our post-pandemic world, contract research organizations (CROs) face more challenges than ever. With greater competition, market consolidation, and a growing emphasis on site empowerment, the CRO market is in a state of flux. Only those willing to be flexible as they apply learnings from the COVID-19 pandemic and its aftermath are likely to come … Read more

Template Building Service

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Template Building Service Save time, ensure regulatory compliance and produce excellent data! Saves your team valuable time that can be re-purposed for other critical tasks Provides a proper foundation for excellent CTMS financial and visit tracking Ensures compliance with accurate templates that align protocol timelines and windows Captures ALL study finances with expert help to … Read more