Slideshow: First-in-Man Patient Studies See Quicker Enrollment in Eastern Europe
Lisa Henderson interviews Gerd Arold of PRA about patient enrollment in early phase trials in Eastern Europe
Data Doubts Cloud Europe's Clinical Trials Hopes
Exco InTouch Formally Receives US - European Union/Swiss Safe Harbor Certification for Data Protection
The Avoca Group Selects Strategic Partner, Sitrof Technologies
Oracle Introduces Oracle Health Sciences Mobile Clinical Research Associate
What Dedication Looks Like
Aptuit Offers Design, Implementation and Analysis of Imaging Brain Studies
SGS Expands Viral Challenge Testing Facility Within Its Clinical Unit In Antwerp - Belgium
Promise - and Problems - Signal Mixed Year Ahead for Big Pharma
Small Clinical Trials Feasible for New Limited-Population Approval Pathway
Spaulding Clinical Research Expands Clinical Pharmacology Facility With 12-Bed First-In-Human, High-Visibility Unit
Quintiles Files Registration Statement for Initial Public Offering
OIG Says FDA Lacks Comprehensive REMS Data
CROMSOURCE Further Expands Polish Operations
Resolving The Conflict Over Surging Clinical Trial Costs & Sluggish Enrollment
The Sunshine Act Final Ruling: Clarification for Clinical Research
K&L Consulting Services, Inc. of Fort Washington, PA Selects OpenClinica Enterprise Clinical Trial Software
BBK Worldwide Launches Expanded Suite Of Retention Products To Support Clinical Trial Study Sites
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 4-7 February 2013
OpenClinica Announces 2013 Global Conference
Uncovering Enrollment Underperformance via Business Analytics
Oracle Unveils New Version of Oracle Health Sciences ClearTrial Plan and Source Cloud Service
Exco InTouch Joins Critical Path Institute ePRO Consortium to Advance Electronic Data Capture in Clinical Trials
Phase I Trials Take on Greater Budgetary Importance
ERT, Johns Hopkins University and the University of Washington Expand Study on Effects of Home-Health Monitoring on Exacerbations of Cystic Fibrosis
Avoca Quality Consortium Announces 2013 Key Initiatives
CRF Health's TrialMax ePRO Instrument Achieves Validation Standard
Regulatory Landscape Changes in Russia
Russian regulators have reportedly implemented the much awaited changes to the nation's regulatory process for medical devices, and the revised regulations took effect at the start of January.
Cutting Our Losses in Translation
To reduce the time from bench to bedside we need to transform competition into cooperation.
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