Insights
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Cell & Gene Therapy
How should we handle financial conflicts of interest in FDA-regulated clinical trials?
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FDA & ICH
What are the signature requirements for translated informed consent documents?
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Series: Ask the IRB & IBC Experts
Can participants be reconsented over the phone when an ICF is updated?
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FDA & ICH
What are the IRB submission requirements for observational studies?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5d028075a813c.jpg)
Questions on regulations for process development and purchased human cells
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2019/06/review-sign-document-doctor.png)
Regulatory Compliance
What training documentation is required for conducting clinical research studies?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2019/06/elderly-patient-consultation.jpg)
What are ethical considerations for a trial with a pre-study washout period?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2019/06/f6fef22fd9dd5d9865c0177ca0c0cbb8d1414d9c.jpg)
Stump the Experts: Patient Recruitment Q&A
Videos![](https://www.wcgclinical.com/wp-content/uploads/2019/05/shutterstock_276187949.jpg)
Virtual Clinical Trials: Best Practices in Moving Toward a Patient-Centric Research Model
Whitepapers![](https://www.wcgclinical.com/wp-content/uploads/2022/03/get-under-the-hood-while-the-trial-is-running-identify-and-rectify-data-problems-before-its-too-late.png)