Regulatory Compliance
Clinical Trial Safety
WCG IRB Central and Institutional Site Relationships
Case Studies
Ethics in Clinical Research
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
Whitepapers
Ethics in Clinical Research
What are the requirements for notifications of study closure at research sites?
Blog Posts
Ethics in Clinical Research
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts
FDA & ICH
Does my customer survey project require IRB review?
Blog Posts
COVID-19
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts
Cell & Gene Therapy
The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
Whitepapers
Diversity & Inclusion
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
Whitepapers
Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers
Participant Recruitment