Scilife AMA Session | How to survive and thrive in FDA and EU inspections for GxP - Ask the expert
Got GxP inspection questions? Ask an expert LIVE! 🎙️
We know FDA, EMA, and MHRA inspections can be tough. That’s why we’re bringing in Andres Gola, a Senior Consultant at PBSV with 15 years of experience in GMP, quality systems, and compliance, to answer your questions in a live AMA!
Why guess and stress over how to prepare for GxP inspections when you can get answers straight from a seasoned auditor?
We’re bringing in an expert with years of experience in the FDA and EU-regulated life sciences environments and industry to answer all your questions—no guesswork is required.
Now’s your chance to ask an experienced auditor about:
- Regulatory differences between FDA, EMA, and MHRA inspectors
- Preparing for a GxP inspection
- Managing inspections effectively
- Handling findings and ensuring long-term compliance
- The future of regulatory audits
You'll get insights from Andres Gola, Senior Consultant at PBSV, with 15 years of experience in FDA-regulated environments, specializing in quality systems, GMP, and FDA inspections.
Angel Buendía, Scilife’s Knowledge Manager, will be moderating this online session.
📅 April 3rd, 2025 | 11:00H (CET)
This is a one-time exclusive event that you won’t want to miss.
P.S. To make the most of this session, submit your questions when you register!