Scilife Showcase | Avoiding FDA Form 483: Streamlining supplier qualification with Scilife
Supplier qualification mistakes happen more often than you think—and the cost is high. ⚠️
Regret won’t fix a compliance mistake, but the right approach will!
Join our webinar to learn how to avoid FDA 483s with smarter supplier management.
Staying FDA-compliant isn’t easy, especially when one supplier mistake could land you a Form 483.
The good news? Avoiding it is easier than you think.
Join Scilife’s upcoming webinar to see how their platform simplifies supplier qualification, helping you document every step of the process, so you’re always audit-ready with a fully compliant supplier management program.
Showcase | Avoiding FDA Form 483: Streamlining supplier qualification with Scilife
March 27, 2025 | 11:00H (CET)
What you’ll learn:
- Efficiently create and manage supplier questionnaires within Scilife.
- Perform robust quality assessments based on supplier data.
- Use Scilife's tagging system to categorize suppliers based on risk.
- Document every step of the supplier qualification process.
Plus, we’ll go through common observations cited in FDA 483 forms related to supplier qualification.
The dreaded FDA form 483 is avoidable when you have the right strategies and tools at your fingertips.