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Compliance Fire Drill: Mock FDA Audits for Cleaning Validation

June 19, 2024 Eliza Deriso
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In this Pharma Manufacturing article, Director of Consulting and the Compliance Center of Excellence at Azzur Group, Eliza Deriso, provides insight on worst-case products for one of the most common places the FDA finds violations - cleaning validation. She details the key steps and priorities you should be including in your mock audit to prevent warning letters from the FDA.

“By conducting mock inspections, companies can understand any potential problem areas and to deal with those problems before they are noted in a real inspection.” - Eliza Deriso, Director of Consulting and the Compliance Center of Excellence at Azzur Group

Read the full article by Eliza featured on Pharma Manufacturing to make your next FDA inspection a success.


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Eliza Deriso

Eliza Deriso is a seasoned professional with a strong background in quality management and auditing. With a career spanning over a decade in both the automotive and life science industries, Eliza has amassed extensive experience in driving quality initiatives. Following a transition from the automotive sector to the life science industry, Eliza joined Azzur Group in 2021, and now leads an audit program that encompasses GMP, GLP, GCP, Medical Device, and Mock FDA audits, among others.
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