December 5-9, 2016 at Atlantic City, New Jersey
The 72nd Deming Conference on Applied Statistics
Sponsored by Metropolitan Section, ASQ and Biopharmaceutical Section, ASA
   
2016 Program
      


Program Tutorial Sessions Short Courses Poster Session
Student Award Book Sale Download Program Abstract Submission
ASA Biopharmaceutical Section
and Deming Scholar Award
Biopharm-Deming Scholar Award
Application Form
Download Presentation Slides

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 72nd Deming Conference will be held on December 5-9, 2016 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. Click here to download the complete program pdf file.

      

The 72nd Deming Conference Program
Poster sessions will be in the middle of the 3 extended tutorial sessions (Monday afternoon, and Tuesday and Wednesday Morning)
12/5/2016 (Monday)
Morning Session (8:30 AM - 11:30) Afternoon Session (1:15 PM - 4:30 PM)
Session A: Data display for statistical analysis &

Prof. Richard Heiberger
Temple University

Session C: Dose-Response Design and Analysis in Drug Development &

Dr. Richard C. Zink
SAS Institue


Dr. Sandeep Menon
Pfizer Inc

Session B: Non-inferiority testing in clinical trials: issues and challenges &

Dr. Tie-Hua Ng
FDA

Session D: Benefit-risk assessment methods in medical product development: bridging qualitative and quantitative assessments &

Dr. Qi Jiang
Amgen


Dr. Weili He
Merck

7:00 PM: Speaker Dinner and Student Poster Award
12/6/2016 (Tuesday)
Morning Session (8:30 AM - 11:45 AM) Afternoon Session (1:15 PM - 4:15 PM)
Session E: Biomarker evaluation and subgroup discovery in clinical trials

Dr. Ilya Lipkovich
Quitiles


Dr. Alex Dmitrienko
Mediana Inc.

Session G: Quantitative sciences for safety monitoring in clinical development
(On Behalf of the ASA Safety Monitoring Working Group)


Mr. Rober 'Mac' Gordon
JNJ


Ms. Judy X. Li
FDA


Dr. William Wang
Merck

Session F: Basic multiple comparisons in clinical trials and genomics

Dr. Bushi Wang
Boehringer Ingelheim Pharmaceuticals, Inc


Prof. Xinping Cui
University of California

Session H: Improving our understanding of “less well-understood” adaptive trials: challenges, best practices and sharing of case studies

Dr. Eva Miller
Independent Statistical Consultant


Dr. Weili He
Merck

12/7/2016 (Wednesday)
Morning Session (8:30 AM - 11:45 AM) Afternoon Session (1:15 PM - 4:15 PM)
Session I: Simulation-based approaches to clinical trial design and analysis

Dr. Alex Dmitrienko
Mediana Inc.

Session K: Regulatory statistics with some European perspectives

Prof. Franz König
Medical University of Vienna


Prof. Martin Posch
Medical University of Vienna


Dr. Frank Bretz
Novartis Pharma AG

Session J: Design of dose-response clinical Trials &

Dr. Naitee Ting
Boehringer-Ingelheim Pharmaceuticals Inc.

Session L: Quantitative methods for traditional chinese medicine development &

Prof. Shein-Chung Chow
Duke University School of Medicine

12/8/2016 - 12/9/2016 (Thursday and Friday)
8:00 – 9:30: Lecture / 9:30 – 9:50: Break / 9:50 – 11:20: Lecture / 11:20 – 12:40: Lunch / 12:40 – 2:10: Lecture / 2:10 – 2:30: Break / 2:30 – 4:00: Lecture / 4:00 - 4:20: Break / 4:20 - 5:50: Lecture
There will be 5 lectures on Thursday and 3 on Friday so one can book an earlier flight. The Friday luncheon will be a 40-minute refreshment break.
Short Course 1: Adaptive designs and multiple testing &

Prof. Franz König
Medical University of Vienna


Prof. Martin Posch
Medical University of Vienna


Dr. Frank Bretz
Novartis Pharma AG

Short Course 2: Bioequivalence, Biosimilars, & Statistics in Clinical Pharmacology &

Dr. Scott Patterson
Pfizer Inc


Dr. Byron Jones
Novartis Pharma AG


Ms. Johanna Mielke
PhD Candidate, Novartis Pharma AG.


 
The following books will be used and sold during the conference. Please order the books through the registration page. You should not order the book used for the short course you registered unless you want to order extra copies.
Book Information (Author, Title, etc.) Price (USD)
List Discount
Taylor and Francis
Tie-Hua Ng, Noninferiority Testing in Clinical Trials: Issues and Challenges, 2014, 208 Pages, ISBN: 978146656149679.95 51
Qi Jiang, and Weili He, Benefit-Risk Assessment Methods in Medical Product Development: Bridging Qualitative and Quantitative Assessments, 2016, 296 Pages, ISBN: 978148225936099.95 63
Shein-Chung Chow, Quantitative Methods for Traditional Chinese Medicine Development, 2015, 430 Pages, ISBN: 9781482235999119.95 75
Scott D. Patterson, and Byron Jones, Bioequivalence and Statistics in Clinical Pharmacology (2nd Edition), 2016, 480 Pages, ISBN: 9781466585201 (Included in Short Course 2) 119.95 75
Springer
Richard M. Heiberger, and Burt Holland, Statistical Analysis and Data Display - An Intermediate Course with Examples in R (2nd Edition), 2015, 898 Pages, ISBN: 978-1-4939-2121-879.99 52
Gernot Wassmer, and Werner Brannath, Group Sequential and Confirmatory Adaptive Designs in Clinical Trials, 2016, 301 Pages, ISBN: 978-3-319-32560-6 (Recommended by instructors and included in Short Course 1) 129 80
Naitee Ting (Editor), Dose Finding in Drug Development, 2006, 248 Pages, ISBN: 978-0387-29074-4209 128
SAS Institute
Sandeep Menon, and Richard C. Zink, Modern Approaches to Clinical Trials Using SAS®: Classical, Adaptive, and Bayesian Methods, 2015, 364 Pages, ISBN: 978-1-62959-385-269.95 45