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news roundup
The Coalition for Clinical Trials Awareness will host a Capitol Hill policy roundtable featuring industry professionals on Wednesday, May 3. This event is part of the nationwide Clinical Trials Awareness Week taking place from May 1-5.
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Transform Clinical Trials with Better Data Collection
Managing clinical data in a modern EDC gives deeper insights so teams can make better decisions faster. Learn how --
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Bioclinica AGILE RTMS is the company's configurable randomization and trial supply management (RTSM) software platform to provide seamless clinical supply forecasting and management together with IRT. The RTSM platform combines the latest release of Bioclinica's Trident Agile IRT and the advanced Optimizer clinical supply forecasting and management software.
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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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ACRP and DrugDev have announced a partnership to offer ACRP clinical researchers and site staff members online profiles visible to pharma companies and CROs.
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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
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Greenphire and the Society for Clinical Research Sites (SCRS) released a new survey that revealed the negative impact that manual payment processes have on global clinical research.
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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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Is Your CTMS Working for You? Unify and Optimize Your Approach to Clinical Trials
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Blog Posts
Nora Belcher, executive director at the Texas eHealth Alliance discusses how Health Information Technology (HealthIT) will change the clinical trials landscape.
To get a feeling of how much emphasis is put on ethical review in the Regulation (EU) 536/2014 (CTR), a simple comparison was performed with the current legal document regulating clinical trials, known as the Directive 2001/20/EC (CTD).
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Articles
The implementation of data standards such as IDMP is simply one key step to ensuring that product information is identified and captured accurately within the regulatory framework and beyond.
Our expert committee offers advice for improving outsourcing relationships and their efficiencies.
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