Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Five Tips for Creating & Negotiating the Best Clinical Trial Budget for Your Site
Blog Posts
Clinical Trial Operations
Emerging Challenges in Oncology Trials: Enrollment, Protocol Deviations, and Growing Data
Blog Posts
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 PostsWhat Are Clinical Trials and How Do They Benefit Participants?
Blog Posts
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
Ethics in Clinical Research
What questions can be asked when screening patients prior to them signing consent?
Blog Posts
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
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
Clinical Endpoints