Content Contributor Susan Leister

Susan Leister, BS, MBA, PhD, CQA, CSSBB

Technical Resources International Inc. & University of Phoenix

Dr. Susan Leister serves as the Vice-President of Quality and Compliance at Technical Resources International Inc. and faculty for the University of Phoenix in both graduate and undergraduate studies with over 20 years of experience in the pharmaceutical, biotech, and medical device industry. She has a Bachelor’s Degree in Biochemistry and Molecular Biology, an MBA, a Doctorate in Organization & Management with a focus in Leadership, and holds certifications from ASQ as Certified Quality Auditor and Six Sigma Black Belt. She has broad experience in GXP and has led numerous regulatory inspections and built quality systems from the ground up.

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FDA Inspections: From Site Preparation to Response

Featured

Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.

FDA Inspections: From Site Preparation to Response
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Good Manufacturing Practices (GMP)

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An in-depth introduction to GMP for pharmaceuticals.

Good Manufacturing Practices (GMP)
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Comprehensive CRC

CME/CEUFeatured

Provides clinical research professionals with basic and advanced training tailored to the CRC’s critical role in the conduct of clinical trials.

Comprehensive CRC

Clinical Research Coordinator (CRC) Advanced

CME/CEU

This course provides clinical research professionals with advanced training tailored to the CRC’s critical role in the conduct of clinical trials.

Clinical Research Coordinator (CRC) Advanced