Oncology
![](https://www.wcgclinical.com/wp-content/uploads/2021/02/scientist-pipette-gene-transfer.jpg)
Cell & Gene Therapy
Does Human Gene Transfer research at my site require IBC approval?
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FDA & ICH
When should a child assent form be used in a pediatric clinical trial?
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Providing Research Participants with New Information: Is “Re-Consent” Always Necessary?
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Clinical Trial Safety
What are IRB submission requirements for post marketing safety reports?
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Ethics in Clinical Research
May I pay a physician for referring a patient to our study?
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Institutional Biosafety Committee Review for Genetically Modified Vaccines and Gene Transfer Products
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Clinical Trial Safety
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/03/informed-consent-an-irb-perspective-on-navigating-the-new-normal.jpeg)
COVID-19
Informed Consent: An IRB Perspective on Navigating the New Normal
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Series: Ask the IRB & IBC Experts
What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
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COVID-19