Oncology
FDA & ICH
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
Clinical Endpoints
WCG Supports Small Oncology Biotech Through Rapid Growth, Saving Hundreds of Thousands of Dollars
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
Whitepaper – The Power of More Re-Imagining the Traditional Business Model for Oncology Clinical Research
Whitepapers
Clinical Endpoints
See How WCG Helped a Mid-tier Biopharma Respond to an Urgent FDA Request, and Adjudicated 400 Endpoints in Just a Few Short Weeks
Case Studies
Ethics in Clinical Research
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
COVID-19
Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment
Case Studies
Participant Recruitment