Biotech Leaders
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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?
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Questions on regulations for process development and purchased human cells
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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?
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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/2020/07/itemeditorimage_5ced66da41c73.jpg)
Regulatory Compliance
How to resolve irregularities in the documentation of informed consent?
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Ethics in Clinical Research
Can the IRB approve reimbursement of copays for routine costs in a clinical trial?
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Regulatory Compliance