Biotech Leaders
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
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Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Clinical Endpoints
Small Biotech Saves More Than $12k Monthly with WCG Safety Solutions
Case Studies
Clinical Endpoints
A Successful DMC Requires a Productive, Early Organizational Meeting
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Clinical Endpoints
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers
Clinical Endpoints
Tips For A Successful Organizational DMC Meeting
Videos
FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
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Ethics in Clinical Research
Compensating Research Participants FAQ
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