Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
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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/2022/03/get-under-the-hood-while-the-trial-is-running-identify-and-rectify-data-problems-before-its-too-late.png)
Get under the hood while the trial is running: Identify and rectify data problems before it’s too late
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5ced66da41c73.jpg)
Regulatory Compliance
How to resolve irregularities in the documentation of informed consent?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5cdad64d2b6d8.jpg)
Ethics in Clinical Research
Can the IRB approve reimbursement of copays for routine costs in a clinical trial?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5cd4971b7f8dc.jpg)
Regulatory Compliance
Is IRB review required for survey results that may be published?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5cd307106b239.jpg)
What are the requirements for submitting protocol deviations?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5cc8758904dc8.jpg)
Regulatory Compliance