Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
What is the IRB’s responsibility for the review of updated Investigator Brochures?
Blog Posts
Ethics in Clinical Research
If a Subject’s Care Is Divided Equally Between Two Caregivers, Who Should Sign Caregiver Consent?
Blog Posts
Regulatory Compliance
Can we charge a subject for a diagnostic test not done as part of the IRB approved protocol?
Blog PostsIs it ethical to pay subjects for referring friends to a clinical research site?
Blog Posts
Regulatory Compliance
How should a site document a missing signature on a HIPAA authorization form?
Blog PostsIn the Gut, In the Environment, On the iPad: Emerging Developments in Autism Research
Blog PostsLessons Learned from 600+ Expert Committee Members
Blog Posts
Clinical Trial Operations
Preparing for Success: A Better Way to Manage the Feasibility Process
Blog Posts
Clinical Endpoints
How Calibrated Are Your Trial-Measurement Tools?
Blog Posts
Clinical Trial Safety