Live on Wednesday, August 12 at 8 AM PST
Your regulated footprint doesn't stop at your own facility. It extends into every CRO, CMO, and supplier your product depends on. Sites you do select, but don't control and can't audit as often as you'd like.
This webinar will draw on Redica's Site Intelligence Cloud, covering inspection and enforcement data across 10 health authorities since 2022. We'll break down how third-party site risk accumulates outside your own inspection record and introduce a rebuilt HA Risk Score, AI-driven severity classification, and predictive Warning Letter and CRL risk models now live in the platform. We'll also walk through a real site's 24-year scoring history to show exactly how risk builds, and why recent compliance can outweigh a mixed past.
In this webinar, you will learn:
Designed for Quality, Regulatory, and Supply Chain leaders at small and emerging pharma companies, this session will show how continuous site intelligence can help you move from periodic audits to proactive oversight of the sites your product depends on.

SVP of Quality Intelligence