Ethics in Clinical Research
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
Ethical and Regulatory Considerations in Patient-to-Patient-Referral Recruitment Plans
Whitepapers
Ethics in Clinical Research
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts
COVID-19
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts
Ethics in Clinical Research
FDA Guidance Portal
Resource Hub
Cell & Gene Therapy
The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
Whitepapers
Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers
Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Cell & Gene Therapy