Recording of February 18 2023 presentation

Treena Jackson has more than 20 years of experience in diverse areas of the drug development process, including working as a chronic toxicology biologist, and in GLP/ GCP auditing, risk management, regulatory affairs and overall Quality System Management. She has held positions in pharmaceutical companies, CROs and served as a quality management consultant. She has worked with many clients to develop customized SOPs and to develop or strengthen quality management systems for their companies and institutions. Ms. Jackson has developed and delivered orientation and training programs on a wide variety of topics. She’s the contributing author to several regulatory textbooks including “Fundamentals of International Regulatory Affairs.” In addition, Ms. Jackson performs GCP and GLP quality assurance audits for sponsors, CROs, study site personnel, and IRBs. Ms. Jackson is a member of several professional societies. She has taught as an adjunct faculty member at Campbell University in the graduate and undergraduate clinical research program where she developed an online course for Pharmaceutical Compliance. She continues to teach online in various platforms. She has a BS degree in Laboratory Animal Science and an undergraduate Certificate in Biotechnology, a MS degree in Quality Assurance and Regulatory Affairs, a MA degree in Christian Education and is currently working on a PhD in Organizational Leadership. Additionally she holds several certifications including Certified Quality Auditor, Certified Regulatory Affairs Professional, and Certified Six Sigma Green Belt. She has worked in Pharmaceutical Executive levels of Quality for several organizations and most recently led the Quality effort leading to the approval of a novel breast cancer treatment. She is the president and Founder of Quality Resource Consulting, Inc.