Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
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FDA & ICH
When should a child assent form be used in a pediatric clinical trial?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/12/report-review.jpg)
Clinical Trial Safety
What are IRB submission requirements for post marketing safety reports?
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Ethics in Clinical Research
May I pay a physician for referring a patient to our study?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/06/Thumb_Pediatric-Drug-Development-The-EuroPerspectivepean.png)
Clinical Endpoints
Regulatory Challenges in Pediatric Drug Development: The European Perspective
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/03/best-practices-for-research-sites-effectively-using-patient-recruitment-advertising-dollars.png)
Best Practices for Research Sites: Effectively Using Patient Recruitment Advertising Dollars
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/10/shutterstock_1639731790-1-scaled.jpg)
Clinical Endpoints
Using eCOA to Improve Data Quality in Parkinson’s Disease Clinical Trials
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/03/data-and-biorepository-management-during-a-pandemic.jpeg)
COVID-19
Data and Biorepository Management During a Pandemic
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/06/Thumb_Improving-Data-Quality-for-a-Critical-Multiple-Sclerosis-Endpoint.png)
Clinical Endpoints
Improving Data Quality for a Critical Multiple Sclerosis Endpoint
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5f109f472e55e.png)
Clinical Trial Safety
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2022/03/informed-consent-an-irb-perspective-on-navigating-the-new-normal.jpeg)
COVID-19