December 4-8, 2017 at Atlantic City, New Jersey
The 73rd Deming Conference on Applied Statistics
Sponsored by Metropolitan Section, ASQ and Biopharmaceutical Section, ASA
   
2017 Program
      


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Abstract Submission (will open on August 15) Download Presentation Slides ASA Biopharmaceutical Section
and Deming Scholar Award
Biopharm-Deming Scholar Award
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The purpose of the 3-day Deming Conference on Applied Statistics is to provide a learning experience on recent developments in statistical methodologies. The conference is composed of 12 3-hour tutorials on current statistical topics of interest based on recently published texts. The conference is followed by two 2-day parallel short courses. The conference sells these books at a 40% discount. Poster submissions are also solicited.

Poster Session

The Annual Deming Conference on Applied Statistics will accept submission of abstracts for poster presentation during the conference. The poster sessions provide a forum to attendees to present concepts and issues of relevance to their peers. The rules and tips of the poster presentations can be found by clicking the button below.

or click here to download the pdf file.


Program Summary

The 73rd Deming Conference will be held on December 4-8, 2017 at Atlantic City, NJ. There will be two parallel half-day tutorial sessions based on recently published books for the first three days for a total of 12 tutorial sessions (December 5, 6, 7). Then the conference will continue with two 2-day short courses on December 8 and December 9. The books used for the tutorial sessions and for the short courses as well as books written by invited speakers will be sold at an appreciable discounted prices. The authors of the books are invited as the speakers. Poster sessions will also be presented. A complete program pdf file will be available for download.

 

The 73rd Deming Conference Program
Poster sessions will be in the middle of the 3 extended tutorial sessions
(Monday afternoon, and Tuesday and Wednesday Morning)
Click topic titles for abstracts and speaker names for bios

 
12/4/2017 (Monday)
     6:30 AM - 8:00 AM Registration
 
     7:00 AM - 8:00 PM Full Hot Breakfast (Covered by registration fee)
 
     8:00 AM - 9:00 AM Keynote Session
Roles of Biostatisticians In New Drug Development and Regulatory Review
Dr. Yuki Ando, Senior Scientist for Biostatistics
Pharmaceuticals and Medical Devices Agency, Japan
 
     9:00 AM - 12:00 Noon Session A(based on book)
Hot Topics in Clinical Trials: Multiple Outcomes and Benefit: Risk
Dr. Toshimitsu Hamasaki, National Cerebral and Cardiovascular Center
Dr. Scott R. Evans, Harvard University
 
Session B
Missing Data Analysis Using SAS®
Dr. Frank Liu, Merck & Co. Inc.
Dr. Fang Chen, SAS Institute
 
     12:00 Noon - 1:30 PM Lunch Break (on your own)
 
     1:30 PM - 4:45 PM Session C
Regulatory Science and Drug Development in China
Professor Naiqing Zhao, Fudan University
Dr. Jie Chen, Merck Research Laboratories
 
Session D(based on book)
Phase II Clinical Development of Drugs
Dr. Naitee Ting (Boehringer Ingleheim)
Dr. Shuyen Ho (UCB)
 
     7:00 PM Session Speaker Dinner
Speaker Dinner and Student Awards (optional, fee added)
 
12/5/2017 (Tuesday)
     6:00 AM - 8:00 AM Registration
 
     7:00 AM - 8:00 AM Full Hot Breakfast (Covered by registration fee)
 
     8:00 AM - 9:00 AM Session Keynote
Bridging Study Evaluation and MRCTs in Taiwan: Regulatory Perspectives and Experiences
Dr. Guei-Feng Tsai, Statistical Team Leader
Division of New Drugs, Center for Drug Evaluation; Taiwan
 
     9:00 AM - 12:15 PM Session E(based on book)
Generalized Linear Models
Alan Agresti, Distinguished Professor Emeritus, University of Florida
 
Session F
Likelihood-Based Methods for Continuous Safety Monitoring of Pharmaceutical Products
(On Behalf of the ASA Safety Monitoring Working Group)

Dr. William Wang (Merck),
Dr. Krishan P. Singh (GSK)
Dr. Ram Tiwari (FDA))
On Behalf of the ASA Safety Monitoring Working Group
 
     12:15 PM -1:45 PM Lunch Break (on your own)
 
     1:45 PM - 4:45 PM Session G
Multi-Regional Clinical Trials and the ICH E17
Dr William Wang (Merck)
Dr Yuki Ando (PMDA)
 
Session H
Causal Inference in a Big Data World: Introduction to Parametric and Semi-Parametric Estimators for Causal Inference
Dr. Laura Balzer, Assistant Professor of Biostatistics at the University of Massachusetts, Amherst
 
12/6/2017 (Wednesday)
     6:30 AM - 8:00 AM Registration
 
     7:00 AM - 8:00 AM Full Hot Breakfast (Covered by registration fee)
 
     8:00 AM - 9:00 AM Session Keynote
Regulatory Hot Topics in Europe
Frank Pétavy, Biostatistics and Methodology Support
R&D Division, European Medicines Agency, London, UK
 
     9:00 AM - 12:15 PM Session I
Benefit–Risk Assessment and Utility of Real World Evidence in Medical Product Development and Life Cycle Management
Dr. Weili He, Merck & Co., Inc
Dr. Qi Jiang, Amgen.
 
Session J
Dose-Finding in Clinical Development
Dr. Qiqi Deng, Boehringer Ingleheim
 
     12:15 PM - 1:45 PM Lunch Break (on your own)
 
     1:45 PM - 4:45 PM Session K
Statistical & Strategic Considerations in Development of Oncology Immunotherapies
Dr. Cong Chen, Merk & Co.
 
Session L(based on book)
Meta-Analysis and Network Meta-Analysis in Clinical Trials
Dr. Joseph C. Cappelleri, Pfizer Inc
Prof. Ding-Geng (Din) Chen, University of North Carolina at Chapel Hill
 
12/7/2017 - 12/8/2017 (Thursday and Friday)
     6:30 AM - 8:00 AM Registration
 
     7:00 AM - 8:00 AM Full Hot Breakfast (Covered by Short Course registration fee)
 
     8:00 AM - 5:50 PM (Thu)
     8:00 AM - 1:30 PM (Fri)
Short Course 1
GUIDE Approach to Subgroup Identification and Analysis for Precision Medicine
Prof. Wei-Yin Loh, University of Wisconsin
 
     8:00 AM - 5:50 PM (Thu)
      8:00 AM - 1:30 PM (Fri)
Short Course 2(based on book)
Multiplicity Issues in Clinical Trials
Dr. Alex Dmitrienko, Mediana Inc



Book information will be published later.