Musculoskeletal
![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5d2e0f448ff4b.jpg)
Cell & Gene Therapy
How should we handle financial conflicts of interest in FDA-regulated clinical trials?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5d125d3607757.jpg)
FDA & ICH
What are the signature requirements for translated informed consent documents?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5d125541da3db.jpg)
Series: Ask the IRB & IBC Experts
Can participants be reconsented over the phone when an ICF is updated?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5d03b43880645.jpg)
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/2019/05/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