Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
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 Posts
Is 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 Posts
In the Gut, In the Environment, On the iPad: Emerging Developments in Autism Research
Blog Posts
Lessons 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
What are the IRB Reporting Requirements for Adverse Events?
Blog Posts
Clinical Trial Safety