Ethics in Clinical Research
Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Cell & Gene Therapy
WCG IRB’s Response to COVID-19 in 2020: Supporting the Clinical Trial Industry When It Needed It the Most
Case Studies
Clinical Endpoints
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers
Ethics in Clinical Research
Compensating Research Participants FAQ
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
Ethics in Clinical Research
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
Ethics in Clinical Research
The IRB’s Perspective: Determining Optimal Compensation for Clinical Trial Participants
Whitepapers
COVID-19
Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment
Case Studies
Ethics in Clinical Research