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Drug Safety

adverse event reporting

Adverse Event Reporting Failures That Led to Multi-Billion Dollar Lawsuits

“Discover how adverse event reporting failures result in multi-billion dollar lawsuits and learn from our expert guidance.”

Category : Clinical Medicine Drug Safety, Lawsuits, Pharmaceutical industry Read More
FDA post-market surveillance

What Happens After FDA Approval: The Surveillance You Never Knew Existed

Unlock FDA post-market surveillance insights with NEISS, providing 95%+ accuracy for major injuries and state-by-state availability maps. Contact us for expert help.

Category : Data Collection and Analysis Adverse Event Reporting, Drug Safety, FDA Monitoring, Healthcare compliance, Medical Device Tracking, Pharmaceutical Surveillance, Post-Market Surveillance, Public Health Protection, Regulatory Oversight Read More

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