Oncology
![](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?
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/2023/06/WCG-generic-visual-concept-23.jpg)
Clinical Endpoints
Podcast: The Role of Expert Committees in Clinical Research with guest Jonathan Seltzer, MD, MBA, MA, FACC
Podcasts![](https://www.wcgclinical.com/wp-content/uploads/2023/06/WCG-generic-visual-concept-12.jpg)
Clinical Endpoints