White Papers

Jun 29, 2017
Sponsored Content
By Rho
FDA expects study participants to reflect the demographics of clinically relevant populations. However, current clinical trial populations do not reflect demographics and disease prevalence in the US.
Jun 12, 2017
Sponsored Content
Download the eBook to unlock the results of a recently conducted survey on data and analytics in clinical research. You'll gain a better understanding of where the industry is headed with new methods of cleaning and monitoring trial data, predictive analytics and trial design optimization, patient recruitment and retention and more.
Jun 06, 2017
Sponsored Content
Shipments may experience a range of temperature effects that can impact the stability of a product, leading to temperature excursions that cause the product to become unfit for patient administration, and ultimately, cause rejection. Steps must therefore be taken to reduce the risk of temperature excursions and importantly have the data to support adjudication of the product.
Almac’s Heather Bogle discusses these important and necessary steps in her article ‘Temperature Management – Keep your Cool’ which was recently published in an issue of IPI (International Pharmaceutical Industry).
Jun 06, 2017
Sponsored Content
By ERT
Cardiac safety issues are among the most common reasons for promising drugs being halted in development and failing to launch. So why gamble with site-managed ECG collection? Learn more.
Jun 02, 2017
Sponsored Content
The checks and balances built into today’s sophisticated IRT not only creates efficiencies, but improves patient safety. Get to know the latest automated functions and features that will help speed your complex trial’s progress towards closure.
May 22, 2017
Applied Clinical Trials
The pharmaceutical industry is responsible for the successful execution of hundreds of thousands of trials of new drugs and vaccines. Gene therapy trials are unique, combining established experience and new approaches previously unnecessary for developing new drugs.
May 18, 2017
Sponsored Content
Keeping track – and making sense – of all of the information required by regulatory authorities is more complex than ever. Our teams and technology can handle it all with our Regulatory Information Management (RIM) solution - combining real-time intelligence and a leading-edge publishing platform with expert regulatory teams.
May 10, 2017
Sponsored Content
In an ever-changing, patient-driven market, how are you optimizing your clinical trial data and content? In this white paper, discover how a three-part strategy called Big Data Discovery draws from multiple data sources, to provide interactive reporting and actionable insights that enhance and streamline clinical development.
May 04, 2017
Sponsored Content
This concise white paper will help you understand the recent changes ICH has recently made to the ICH E6 Guideline (R2). Learn how use of a Covance three-tiered risk based management approach can help you comply with the addendum and achieve a more efficient design that improves clinical trial implementation.
May 04, 2017
Sponsored Content
By Rho
An optimal dose is high enough to demonstrate efficacy, yet low enough to minimize safety concerns. This article examines four common study designs used to determine the optimal dose.
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