Simplify compliance and reduce the risk
of FDA 483 findings

Staying FDA-compliant isn’t easy, especially when one supplier mistake could land you a Form 483. The good news? It’s simple to avoid when you have the right knowledge and tools. 

In this webinar, you’ll see firsthand how to use Scilife to efficiently manage supplier questionnaires, perform risk-based assessments, and maintain a fully audit-ready documentation trail—all in one centralized platform.