Clinical Operations
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Regulatory Compliance
How do I handle a deviation in the use of blood specimens collected outside the timeframe?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5e3aed6627cf8.jpg)
Questions on the FDA’s 30-Day IND Review Period and IRB Approval
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Clinical Trial Safety
WCG IBC Services
Solution Overviews![](https://www.wcgclinical.com/wp-content/uploads/2019/07/WCG_Logo.jpg)
WCG Experts to Lead Nine Educational Sessions at the PRIM&R 2019 Advancing Ethical Research Conference
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Series: Ask the IRB & IBC Experts
What are the Blood Draw Guidelines for Phase 1 Clinical Trials?
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Questions on Using Generic Recruitment Flyers at Clinical Trial Sites
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Regulatory Compliance
Guidance on genomic research with deceased patients
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Getting the Most Out of Your Site Selection Strategy
Solution Overviews![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5d83b3618865a.jpg)
What is the IRB’s responsibility for the review of updated Investigator Brochures?
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Ethics in Clinical Research