Modernizing Study Enrollment
Using predictive modeling to combat the challenges of study enrollment.
Raising the Bar on Subject Recruitment
Thought leaders in the subject recruitment field come together to discuss current issues and potential solutions.
New FDA Liaison Opens Up
Hear from the first FDA liaison in the Office of International Programs.
Successful Outsourcing: Tracking Global CRO Usage
New survey captures sponsors changing global usage of, and relationships with, CRO partners.
Simulation: A Critical Tool in Adaptive
How simulation can help in the planning and implementation of adaptive clinical trials.
Medical Device Compliance
A probability sampling assessment by FDA takes a look at compliance in the medical device world.
Pressure Mounts to Involve Elderly
The European intiative of involving elderly in clinical trials picks up the pace as challenges are addressed.
Latin America's Trials Climate
Undertaking clinical studies in this emerging region requires first overcoming natural barriers.
Top 5 Mistakes of RFP Writing
Knowing what you want from a CROs proposal will help make the most of the selection process.
Treating Stress in Patients in Europe
EMEA releases new guideline for studies in PTSD, as new figures depict a lagging EU.
eClinical Software: June 2009
The latest eclinical software in the clinical trials industry.
What Do You Want to Know? A Reader's Survey Tells All
Learn what Applied Clinical Trial's readers told us in our annual reader's survey.
EHRs, EDC, and the Hum of HIMSS
Highlights and insights from a recent gathering of thousands of health care professionals.
Business News
Industry news focusing on the people and organizations who work in the clinical trials profession.
Common Ground for eCTD
Roundtable participants discuss challenges and successes with early eCTD implementation.
Global Supply Chain Management
What managers must know and do to overcome regulatory challenges and avoid hiccups.
Clinical Research Under Scrutiny
Agency officials and sponsors anticipate stiffer oversight of research operations and disclosure requirements.
