Sep 10 | eCliniqua | The U.S. Department of Health and Human Services (HHS) has chosen Medidata’s trial cost benchmark data to support research into current cost data for clinical trials.  

Aug 29 | eCliniqua | GUEST COMMENTARY | Faced with a looming patent cliff, supply-chain issues and dwindling pipelines, Big Pharma has to take a closer look at outsourcing as a way to bolster development and manufacturing strategies. Electing for a leaner approach makes sense for many reasons but several key concerns must be addressed, ranging from innovation to emerging markets.  

Aug 17 | eCliniqua | This year’s annual Barnett Clinical Summit, which will be held this October, will focus on the theme of Optimizing Trial Performance, connecting clinical research experts, sponsors, sites and regulators.    

Aug 6 | eCliniqua | A rapidly expanding French CRO called Quinten is quietly building an impressive client roster as it brings an innovative data mining approach to a broad expanse of the drug development pipeline – from early-stage target identification to its sweet spot in clinical trials and patient stratification.   

Aug 6 | Mass Device | Four House Democrats aim to close loopholes in the U.S. government's clinical trial reporting requirements to ensure that all human studies are publicly disclosed online. The proposed Trial & Experimental Studies Transparency Act would require drug makers to report all studies and results publicly through the ClinicalTrials.gov website.