Overview
Do you work on clinical trial issues and would like to know more about the core scientific principles? Need a review on how to interpret clinical trial results? This webinar will discuss fundamentals of clinical trials. Topics include understanding the basics of clinical trial design and interpretation, how to quickly read published clinical trial results, an overview of types of clinical trials, ranging from superiority to non-inferiority designs, and why participant diversity is important.
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Speakers
Margo Heath-Chiozzi, Senior Vice-President, Regulatory Affairs, Celldex Therapeutics, Inc
Lance L. Shea, Partner, BakerHostetler
Robert J. Temple, Deputy Center Director for Clinical Science, CDER
Moderated by Brian J. Malkin, Partner, McDermott Will & Emery
Summer Learning Series
The Summer Learning Series brings the top thinkers and leaders of our industry to speak on a broad array of topics essential to the food and drug law professional, covering matters that perhaps we all wish we knew a bit more about as we work and converse with clients, colleagues, and the FDA. Join us this June through July and build foundation in the following subjects:
- The Essentials of Clinical Trial Science – Wednesday, June 16
- The Essentials of Statistics for Medical Products Lawyers – Wednesday, June 30
- The Essentials of Tobacco and Nicotine Product Research – Wednesday, July 14
- The Essentials of Machine Learning for Regulatory Attorneys and English Majors – Thursday, July 15
- The Essentials of Food Science – Wednesday, July 21
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LANCE SHEA is a partner at BakerHostetler LLP with focus on legal science advocacy, Mr. Shea represents clients in medical products industries such as drugs, medical devices and biotechnology products. Matters span regulatory (e.g., FDA and EPA) and litigation forums (e.g., federal and state courts) and often involve complex scientific evidence and cutting-edge arguments based on interpretation of scientific studies. In recent regulatory matters, Lance advised clients on assessment of safety signals for prescription drug products, drug postmarketing studies required under Risk Evaluation and Mitigation Strategy (REMS), preparation for cGMP food inspection and efficacy, and safety positions based on epidemiology studies of competing medical device products. In litigation matters, he recently represented drug companies in nationwide dockets of products liability cases and a drug/device company on breach of contract litigation.
MARGO HEATH-CHIOZZI,MD is the Celldex Therapeutics, Senior Vice President of Global Regulatory Affairs. She joined Celldex in October 2017 with over 25 years of experience in senior leadership roles in regulatory sciences, pharmacogenetics and product development within the pharmaceutical industry and as a practicing physician and clinical researcher. Prior to Celldex, she led global regulatory strategy in several business units at Bristol Myers-Squibb including Oncology, Immunology, Virology and Genetically Defined Diseases with successful initial approvals or new indications for nine major products. Prior to BMS she served in roles of increasing responsibility at Abbott Laboratories including Medical Director of Pharmacogenetics and Senior Director of Global Marketed Product Development and Outcomes Research. Before Abbott, she established the HIV Clinical Research Program for the University of Hawaii. Dr. Heath-Chiozzi received her BS and MD degrees from the University of Utah. She completed her internal medicine residency at Duke University and infectious disease fellowship at Harvard University.






















































































