Ethics in Clinical Research
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Ethics in Clinical Research
Should Parents Be Allowed to View their Child’s Survey Responses?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2023/06/WCG-generic-visual-concept-11.jpg)
Clinical Trial Safety
WCG IRB Central and Institutional Site Relationships
Case Studies![](https://www.wcgclinical.com/wp-content/uploads/2022/07/doctor-writing-protocol.jpg)
Ethics in Clinical Research
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
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Ethics in Clinical Research
What are the requirements for notifications of study closure at research sites?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/06/p-to-p-recruitment.jpg)
Ethics in Clinical Research
Ethical and Regulatory Considerations in Patient-to-Patient-Referral Recruitment Plans
Whitepapers![](https://www.wcgclinical.com/wp-content/uploads/2022/05/calendar-30-day-marker.jpg)
Ethics in Clinical Research
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2023/06/WCG-generic-visual-concept-23.jpg)
COVID-19
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/02/expanded-access-doctor-patient.jpg)
Cell & Gene Therapy
The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
Whitepapers![](https://www.wcgclinical.com/wp-content/uploads/2021/12/1shutterstock_1905464644.png)
Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers![](https://www.wcgclinical.com/wp-content/uploads/2021/08/shutterstock_1496521928.png)
Clinical Trial Safety