Blog Posts

Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.

Series: Ask the IRB & IBC Experts

Should Consent Form updates be aligned with Investigator Brochure updates, or wait for next Protocol amendment?

Health Disparities and COVID-19 in Minority Communities

WCG Insights

Patient Perspective: COVID-19, Community, and Plea for Equitable Participation in Clinical Trials

Your Well-Being May Depend on a Clinical Trial: What You Need to Know

Best Practices For Delivering Investigator Training Via Virtual Meetings

COVID-19 Insights from Former FDA Commissioner, Scott Gottlieb, MD

Ethics in Clinical Research

What are the requirements for parental permission (consent) in studies involving children?

What ethical safeguards are needed for research involving observation of group behavior?

Regulatory Compliance

How do I handle a deviation in the use of blood specimens collected outside the timeframe?

Questions on the FDA’s 30-Day IND Review Period and IRB Approval

MAGI 2025

May 18, 2025 - May 21, 2025 @ Boston, MA