Ask the Experts What are the requirements for notifications of study closure at research sites? Read More about What are the requirements for notifications of study closure at research sites?
Whitepapers Ethical and Regulatory Considerations in Patient-to-Patient-Referral Recruitment Plans Read More about Ethical and Regulatory Considerations in Patient-to-Patient-Referral Recruitment Plans
Blog Posts Managing the Shortage of Contrast Agents in Clinical Research Studies Read More about Managing the Shortage of Contrast Agents in Clinical Research Studies
Ask the Experts Can a protocol get IRB approval during the 30-day IND waiting period? Read More about Can a protocol get IRB approval during the 30-day IND waiting period?
Ask the Experts Does my customer survey project require IRB review? Read More about Does my customer survey project require IRB review?
Blog Posts WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic Read More about WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts Using an IRB’s Site Relationships to Relieve “Site Crunch” and Reduce Trial Pressures Read More about Using an IRB’s Site Relationships to Relieve “Site Crunch” and Reduce Trial Pressures
Whitepapers The Basics of the Individual Expanded Access Request Process: A Resource for Physicians Read More about The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
Whitepapers The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation Read More about The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation