
Joan Versaggi, MBA
With over 35 years’ global experience in the pharmaceutical industry, Joan Versaggi has a diverse range of quality, compliance, clinical and business process improvement consulting knowledge and expertise. Versaggi has led teams of quality and compliance professionals in developing and implementing strategic plans to support quality management systems and processes to ensure compliance and adherence to applicable quality standards in clinical research.
Latest Posts by Joan Versaggi

Q&A: FDA Updates: BIMO – What Sponsors Need to Know
Advarra experts Joan Versaggi and Leslie Paul answer questions from the first in the webinar...
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Implementing a Quality Management System
Many research and development (R&D) organizations across the industry have limited access to a quality department...
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Data Integrity – It’s All About the Data!
In this increasingly digital world, we have to remember data is now available in many different medians, including paper. When we think...
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FDA Inspection Readiness: After the Inspection
In the final part of the three-part FDA inspection readiness series, we will go into...
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FDA Inspection Readiness: During an Inspection
In our previous blog, FDA Inspection Readiness: Preparing for an Inspection we reviewed how to...
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