Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Series: Ask the IRB & IBC Experts
Is informed consent needed for post-market patient registry?
Blog Posts
Clinical Trial Operations
The Top Five Things You Need to Know About Hosting Virtual Investigator Training
Blog Posts
Cell & Gene Therapy
Key Takeaways From FDA’s New Draft Guidance, “Studying Multiple Versions of a Cellular or Gene Therapy Product in an Early-Phase Clinical Trial”
Blog Posts
Participant Recruitment
Does the IRB need to approve doctor-to-doctor letters?
Blog Posts
Regulatory Compliance
What are the IRB review requirements for human factors/usability testing?
Blog Posts
Five Tips for Improving Your Site’s Study Start-Up Timelines
Blog Posts
Clinical Endpoints
Choosing Between Provisioned, BYOD, and Hybrid Models for ePRO: Which Is Right for Your Clinical Trial?
Blog Posts
Clinical Endpoints
A Successful DMC Requires a Productive, Early Organizational Meeting
Blog Posts
Five Tips for Creating & Negotiating the Best Clinical Trial Budget for Your Site
Blog Posts
Clinical Trial Operations