Statistics Expert Witnesses in Pennsylvania

The SEAK Expert Witness Directory contains a comprehensive list of statistics expert witnesses who testify, consult and provide litigation support on statistics and related issues. Statistics expert witnesses and consultants on this page may form expert opinions, draft expert witness reports, and provide expert witness testimony at deposition and trial. The issues and subjects these statistics expert witnesses testify regarding may include: Ai/Ml, Bayesian Adaptive Design, Biostatistics, Clinical Trial, Edwards, Epidemiological, FDA, Gilead, Group Sequential Design, Machine Learning, Medical Device, Oncology, Pharmaceutical Statistics, Regulatory Submissions, and Rwe.

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Lei Li

PhD Biostatistician & FDA Clinical Trial Expert

LunarAI LLC

Landenberg, Pennsylvania
Statistics, Medical Devices - biostatistics, FDA, Pharmaceutical Statistics, Sanofi, Edwards, Gilead, AI/ML expert, machine learning, clinical trial, Medical Device, Vaccine, Group Sequential Design, Bayesian Adaptive Design, Statistical Review of Evidence, Oncology, Epidemiological, Regulatory Submissions, Survival Analysis, Statistical Expert Witness, RWE
Lei Li, PhD, is a biostatistician, statistical expert consultant, and former FDA/CDRH statistical reviewer with extensive experience in regulatory statistics, real-world evidence (RWE), medical device submissions, pharmaceutical development, clinical trials, and quantitative model evaluation. He is currently supporting two active expert consulting matters involving statistical evidence review, regulatory and clinical data interpretation, assessment of quantitative methods, and evaluation of model assumptions, uncertainty, and data reliability. At FDA/CDRH, Dr. Li evaluated statistical components of 510(k), PMA, and other medical device submissions; assessed safety and effectiveness evidence; reviewed RWE and post-market studies; and advised on complex statistical issues for regulatory decision-making. His FDA work included evaluation of study design adequacy, endpoint justification, sample-size rationale, bias and confounding, missing data robustness, and interpretation of clinical...
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