Explore product safety testing limitations through NEISS data, operated by CPSC since 1972. Uncover 400,000+ annual injury cases and research opportunities
Why Most Medical Device Problems Never Make It to FDA Reports
“FDA adverse event reporting: A guide to understanding the process, timelines, and significance for medical device manufacturers and researchers.”
How Injury Data Triggers Product Recalls That Save Lives
Discover how product recall injury data from NEISS informs safety regulations, with 400,000+ annual cases and CPSC oversight since 1972.
Research Ethics and Code Compliance: Strategies That Withstood Regulatory Scrutiny
Explore our ultimate guide to research ethics and code compliance, covering regulatory frameworks, participant recruitment, ethical considerations, and effective data management.
Electronic Trial Master Files: Implementation Guide for Regulatory Compliance
Discover how to implement clinical trial master files effectively with our comprehensive guide. Learn regulatory compliance, data management, and best practices.