CNS

Clinical Endpoints
Can Your ePRO for Pediatric Clinical Trials Support Multiple Informants?
Blog Posts
Clinical Endpoints
Tips For A Successful Organizational DMC Meeting
Videos
FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
Ethics in Clinical Research
Compensating Research Participants FAQ
Blog Posts
Movement Disorder Case Study: WCG Services for CNS Trials
Case Studies
Through the Drug Development Looking Glass: Rare Disorders and the Treatment of Pain
Videos
Clinical Endpoints
Recent Innovations and their Regulatory Implications for Multiple Sclerosis Trials Addressed in a Special Issue of the Journal of Clinical Neurophysiology by VeraSci Experts
Blog Posts
AIMS User Guide
Solution Overviews
Ethics in Clinical Research
Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
Blog Posts
FDA & ICH