Former FDA Investigator — International Inspection Cadre
Finn Alexander Slizza
Medical device (QMSR) and biotech specialist who served on FDA's International Inspection Cadre.
- QMSR
- Medical Devices
- Biotechnology
- International
20+ years FDA and industry
Background
Alex Slizza is a former FDA Investigator with more than 20 years of combined FDA and industry experience. His expertise is in the medical device (QMSR) and biotechnology areas.
During his FDA tenure he was a member of the International Inspection Cadre — the group responsible for inspections conducted outside the United States, which gives him a working view of how expectations are applied across sites and regions.
What Finn does on an engagement
- QMSR and device quality system assessment
- Biotechnology manufacturing compliance
- International site quality oversight
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