Insights
Ethics in Clinical Research
Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
Blog Posts
FDA & ICH
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
Series: WCG Patient Forum
Married Couple Face Down Rare Disease Together
Videos
Clinical Endpoints
The Parkinson’s Foundation and the Parkinson’s Study Group Provide Recommendations on Overcoming Challenges in Telehealth for Clinical Research Studies
Blog Posts
Clinical Endpoints
WCG Supports Small Oncology Biotech Through Rapid Growth, Saving Hundreds of Thousands of Dollars
Case Studies
Participant Recruitment
WCG Support Lifts Study Enrollment by 56%
Case Studies
Cell & Gene Therapy
[Video] Institutional Biosafety Committee Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos
IBC Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos
Participant Recruitment
WCG Empowers Oncology Sites to Reach Full Potential
Case Studies
Participant Recruitment