Clinical Operations
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Participant Recruitment
Is IRB review required when linking to clinicaltrials.gov postings on patient advocacy websites and newsletters?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2020/07/itemeditorimage_5ced66da41c73.jpg)
Ethics in Clinical Research
Save 456 Days in IRB Review With a Seamless, Coordinated Submission Process
Case Studies![](https://www.wcgclinical.com/wp-content/uploads/2021/03/teen-patient-mask-600x400-1.jpg)
Ethics in Clinical Research
Do parents need to accompany adolescents at each research-related office visit?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2021/02/document-review-desk.jpg)
Cell & Gene Therapy
As a sponsor, does my HGT clinical trial require IBC approval at all sites?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2021/02/scientist-pipette-gene-transfer.jpg)
Cell & Gene Therapy
Does Human Gene Transfer research at my site require IBC approval?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2021/02/w-320.jpg)
Using Predictable and Efficient Data to Take the Risk Out of Site Selection
Whitepapers![](https://www.wcgclinical.com/wp-content/uploads/2022/03/wcg-predict-case-study-type-2-diabetes.png)
Case Study – Feasibility for Type 2 Diabetes Study
Case Studies![](https://www.wcgclinical.com/wp-content/uploads/2021/02/child-patient-doctor-parent.jpg)
FDA & ICH
When should a child assent form be used in a pediatric clinical trial?
Blog Posts![](https://www.wcgclinical.com/wp-content/uploads/2021/01/nurse-patient-waiting-room-form.jpg)
Providing Research Participants with New Information: Is “Re-Consent” Always Necessary?
Whitepapers![](https://www.wcgclinical.com/wp-content/uploads/2020/12/report-review.jpg)
Clinical Trial Safety