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Joan Versaggi, MBA

Managing Expert, Advarra Consulting Quality CoE, Advarra

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

Blog

Q&A: FDA Updates: BIMO – What Sponsors Need to Know

Advarra experts Joan Versaggi and Leslie Paul answer questions from the webinar- FDA Updates: BIMO – What Sponsors Need to Know.

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5 min. read

Blog

Steps to Implementing a Quality Management System

Read our blog to learn more about quality, its role in clinical research, and how to implement a management plan.

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3 min. read

Blog

Data Integrity – It’s All About the Data!

This blog dives into data integrity in clinical research, including how to obtain and maintain data throughout its lifecycle.

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3 min. read

Blog

FDA Inspection Readiness: After the Inspection

Preparing for an FDA inspection and enabling a site-specific process to support it is important. Learn more about what to expect and implement after an FDA inspection is completed at your institution.

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2 min. read

Blog

FDA Inspection Readiness: During an Inspection

Preparing for an FDA inspection and enabling a site-specific process to support it is important. Learn more about what to know while undergoing an FDA inspection at your institution.

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3 min. read

Blog

3 Essential Elements of Change Management Within Clinical Research Operations At Your Research Site

Learn how to make sure the three critical factors for productive change are equally balanced considerations of your change management efforts.

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4 min. read

Blog

Q&A – The New Normal: Considerations for Restarting Research

Experts answer some of the most popular audience questions from the recent webinar The New Normal: Considerations for Restart Research. Read more:

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7 min. read

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Joan Versaggi, MBA

Latest Posts by Joan

Q&A: FDA Updates: BIMO – What Sponsors Need to Know

Steps to Implementing a Quality Management System

Data Integrity – It’s All About the Data!

FDA Inspection Readiness: After the Inspection

FDA Inspection Readiness: During an Inspection

3 Essential Elements of Change Management Within Clinical Research Operations At Your Research Site

Q&A – The New Normal: Considerations for Restarting Research

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