news roundup
Certara announced the launch of a new solution for preparing, analyzing and submitting pharmacokinectic data in Clinical Data Exchange Standards Consortium (CDISC) format.
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Supply Chain Management for Global Clinical Trials
The increasing complexity of global clinical trials brings with it a need to consider the impact on Clinical Supply Chain Management. Download Almac's latest eBook today to explore the market demands and challenges as well as the solutions available.
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ePatientFinder and Rep Network have announced a partnership that aims to provide clinical trial access to patients nationally.
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Run the Trial You Want
Build a trial around patients, not technology. Learn how a modern EDC helps deliver complex studies and improve data collection in
 this white paper |
Medidata announces the acquisition of eClinical technology company, Mytrus Inc. Medidata will add Mytrus' eConsent solution, Enroll, into the Medidata Clinical Cloud.
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Webinar: Choose the Right Sites, Gain Insights from Predictive Analytics.
Need to cut your patient enrollment time?
Learn how one sponsor cut time to reach target enrollment by 20% using objective data insights.Find out how you can reduce risk, decrease cost and improve site selection decisions now.
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BioPlan Associates has released its updated textbook, A Quick Guide to Clinical Trials, 2nd Edition, which describes the clinical trials process and drug development from an international perspective.
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Winning the RAT race: A new Center of Excellence to drive development of regenerative medicines
Live Webinar: Tuesday, May 2 at 11:00am EDT
 Register now |
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Planning Gene Therapy Research? Prepare for institutional biosafety committee (IBC) Review with these tips from the Biosafety Officer at a leading IRB.
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Talking the Patients' Language – the importance of effective, patient-centered engagement
Live Webinar: Tuesday, June 6 at 8:00am EDT
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Articles
Initial findings from a DIA study of patient-centric initiatives in drug development reveal pharma's desire to move toward true patient-centricity, but approaches to implementation are varied.
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Is Your CTMS Working for You? Unify and Optimize Your Approach to Clinical Trials
Live Webcast: Wednesday, April 26 at 1:00pm EDT
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In today's value-driven healthcare system, real-world studies are increasingly becoming mandated by regulators as a condition of approval for new medicines.
Blog Posts
The adoption of electronic health records by hospitals and providers has increased engagement in Health Information Technology (HealthIT) activities. Nora Belcher of the Texas eHealth Alliance speaks on how HealthIT will change the pharma landscape for drug development.
An international panel of industry experts has concluded that randomized, controlled clinical trials provide the fastest and most reliable way to identify the risks and benefits of treatment candidates for infectious disease outbreaks.
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Risk-Based Monitoring
The industry group Metrics Champion Consortium (MCC) and its member organizations wanted to explore the timeliness of data entry for critical data points by sites, and conducted a survey in this area. This article explores the results.
Justin Stark, Head and Director of Risk-Based Monitoring and Standards at UCB will discuss the RBM toolkit, and advancements in RBM.
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Improving Clinical Trial Transparency, Collaboration and Efficiencies
On Demand
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Cloud-based clinical analytics and software solutions provider, Algorics, has announced the newest release of its risk-based monitoring platform Acuity.
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Use Challenge Trials Effectively in Clinical Studies: Lessons Learned from H3N2 Influenza Virus
On Demand
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CBI's 2nd annual Risk-Based Monitoring Global conference takes place in Barcelona and offers information on implementing efficient RBM methodologies and gain real-life study examples from leading industry experts.
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