Ethics in Clinical Research
WCG Clinical | Insights
What Can Institutions with Local IRBs Do to Prepare for the Proposed FDA Single IRB Mandate?
Whitepapers WCG Clinical | Insights
Reviewing the FDA’s Proposed Informed Consent Rule Changes
Whitepapers WCG Clinical | Insights
Should a Protocol Amendment be Submitted in Advance of Consent Form Changes?
Blog Posts WCG Clinical | Insights
Which comes first – IRB or IBC approval?
Blog Posts WCG Clinical | Insights
Is special safety equipment required for IBC approval?
Blog Posts WCG Clinical | Insights
WCG IRB Central and Institutional Site Relationships
Case Studies WCG Clinical | Insights
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
Whitepapers WCG Clinical | Insights
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts WCG Clinical | Insights
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts WCG Clinical | Insights