Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Regulatory Innovation
FDA’s Proposed Rule for Single IRB Review in Cooperative Research
Blog Posts
Regulatory Innovation
FDA’s Single IRB Requirement, Expected but Not Guaranteed in 2025
Blog Posts
Ethics in Clinical Research
Do You Need to Submit an Updated Protocol to the IBC After Already Receiving Approval?
Blog Posts
Hybrid & Decentralized Trials
Decentralized Trials: Thoughts for Sponsors, Investigators, and IRBs
Blog Posts
Ethics in Clinical Research
Compounded Drugs in Research: Navigating IND Exemptions and Current Regulations
Blog Posts
Ethics in Clinical Research
Answering FAQs on HIPAA & PHI: Protect Participants’ Privacy & Ensure Compliance
Blog Posts
Ethics in Clinical Research
The Upcoming sIRB Mandate and the Critical Role of Site Selection: Your Questions Answered
Blog Posts
Noncompliance: Now What? CAPA Principles and Best Practices in Clinical Research
Blog Posts
Clinical Trial Operations
Oversee investigator training and safety reporting for every site and study – with a single login
Blog Posts
Clinical Endpoints