All Insights

Ethics in Clinical Research

WCG Clinical | Insights

Research and Cannabis: Ethical Research in a Changing Regulatory Landscape

Whitepapers

WCG Clinical | Insights

What Can Institutions with Local IRBs Do to Prepare for the Proposed FDA Single IRB Mandate?

Whitepapers

WCG Clinical | Insights

WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic

Blog Posts

MAGI@home 2026

October 19, 2026 @ 10:00AM EDT - October 23, 2026 @ 3:00PM EDT

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Study Planning & Review

Study Enablement

Data & Insights

Study Planning & Review

Site Enablement

Data & Insights

Hematology/Oncology

Central Nervous System

Cardiovascular

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Dermatology

Immunology

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Ethics in Clinical Research

Research and Cannabis: Ethical Research in a Changing Regulatory Landscape

What Can Institutions with Local IRBs Do to Prepare for the Proposed FDA Single IRB Mandate?

Reviewing the FDA’s Proposed Informed Consent Rule Changes

Should a Protocol Amendment be Submitted in Advance of Consent Form Changes?

Which comes first – IRB or IBC approval?

Is special safety equipment required for IBC approval?

WCG IRB Central and Institutional Site Relationships

How to Draft a Research Plan for IRB Review: A Step-by-Step Guide

Can a protocol get IRB approval during the 30-day IND waiting period?

WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic

MAGI@home 2026