Gastroenterology
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
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
Ethics in Clinical Research
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
COVID-19
Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment
Case Studies
Participant Recruitment
Is IRB review required when linking to clinicaltrials.gov postings on patient advocacy websites and newsletters?
Blog Posts
Ethics in Clinical Research
Save 456 Days in IRB Review With a Seamless, Coordinated Submission Process
Case Studies
Ethics in Clinical Research
Do parents need to accompany adolescents at each research-related office visit?
Blog Posts
Cell & Gene Therapy