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Going All-in on ePRO
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Going All-in on ePRO

The growing complexity of clinical trials has fuelled demand for ePRO solutions that ease the burden of trial participation for patients while building confidence in ...
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BYOD, ePRO and Unified Data Management Solutions
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BYOD, ePRO and Unified Data Management Solutions

This article will examine the other advantages of having a unified data management solution. BYOD and ePRO certainly benefit from this, but it does not stop there; ha...
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Clinical Trial Logistics: GCP as an Obstacle Rather than a Support?
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Clinical Trial Logistics: GCP as an Obstacle Rather than a Support?

Within the following white paper Dr Wolfgang Eglmeier, Head, Center for Clinical Trials, Witten/Herdecke University, looks into clinical trials information – from the...
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Precision Power Helps Drive the Drug Development Process for Speciality Medicines
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Precision Power Helps Drive the Drug Development Process for Speciality Medicines

Innovation is the ultimate engine of growth for the global provision of medicines. Speed to market through faster drug development processes is continually in demand,...
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Going All-in on ePro
Special Features

Going All-in on ePro

The growing complexity of clinical trials has fuelled demand for ePRO solutions that ease the burden of trial participation for patients while building confidence in ...
Continue Reading →
Assay Sensitivity in QT Assessment
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Assay Sensitivity in QT Assessment

The TQT study, since its implementation in 2005, has been a target for criticism due to the increased cost of drug development. For the last 10 years, more efficie...
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Evolution of the Proarrhythmic Cardiac Safety Regulatory Landscape: The Likely Revision of ICH Guideline E14 and its Consequences
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Evolution of the Proarrhythmic Cardiac Safety Regulatory Landscape: The Likely Revision of ICH Guideline E14 and its Consequences

Since its release 10 years ago, ICH Guideline E14 has governed the clinical proarrhythmic cardiac safety regulatory landscape: it has been adopted by the United St...
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