September 4-5, 2015
Data Analysis
09. Adverse Event Data Programming for Infant Nutrition Trials
Ganesh Lekurwale and Parag Wani
10. A proposal for intervention and event partial date time imputation
Zhao Chunpeng
39. Detecting Suspected Fraudulent Data in Clinical Trials
(No paper available)
Xiaodong SHI
42. SAS Bayesian Procedure Applications in Clinical Trials
(No paper available)
Aijun Gao
43. Cutpoint Determination Methods in Survival Analysis using SAS®: Updated %FINDCUT macro
(No paper available)
Jayawant Mandrekar and Jeffrey Meyers
75. Not Just Merge - Complex Derivation Made Easy by Hash Object
Lu Zhang
Data Visualization and Graphics
28. A Fully Automated Approach to Concatenate RTF outputs and Create TOC
Zhiping Yan and Lugang Larry Xie
53. GTL makes it is possible: A picture is worth a thousand words
(No paper available)
Lynda Li
62. Build Child Growth Charts Using SAS GTL
Rajesh Moorakonda
Management & Career Development
05. Getting clouds moving across the Pacific - a case study on working with a Chinese CRO on SAS® Drug Development
Chen Shi
32. Developing Global Clinical Programming Team with Qualification and Cost Minimization in China
Margaret Li and Lulu Swei
41. How to Build an “Offshore” Team with “Onshore” Quality
Lulu Swei and Margaret Li
49. Job-Oriented Training Program for Clinical SAS Programmers -- One Year Later
(No paper available)
lixiang yao
52. Managing the analysis programming effort for an NDA submission
Yu Cheng and Quan Zhou
Preparation & Regulatory Standards including CDISC
03. Clinical Data Transparency and Sharing: Update on Research Benefits, Risks and the Future
(No paper available)
Matt Becker
20. Summary level clinical site data for data integrity review and inspection planning in NDA and BLA submission
(No paper available)
Jingwei Gao and Nancy Bauer
24. How to validate clinical data more efficiently with SAS Clinical Standards Toolkit
Vivian Feng
25. Multilingual data support in Dataset-XML with SAS® Clinical Data Integration
Jing Gao
27. SDTM Electronic Submissions to FDA: Guidelines and Best Practices
Christina Chang and Kyle Chang
29. SAS® End-to-End solutions in Clinical Trial
Emma Liu
30. Generating Define.xml Using SAS® By Element-by-Element And Domain-by-Domian Mechanism
Lina Qin
37. Tips for efficient CDISC eCRT production
Lanting Li, Yu Zhu, Yuejuan Meng and Huan Zhu
60. Automatic generating blankcrf.pdf for Rave Study
Haiqiang Luo
63. Reading and Resolving OpenCIDSC Message
Yu Pang
64. STATISTICS AND PROGRAMMING IN THE GLOBALLY EVOLVING LANDSCAPE OF CLINICAL TRIAL REGISTRATION AND RESULTS (CTRR) DISCLOSURE
Paul Ngai and Joyce Hauze
66. Generic Macros for Data Mapping
Qian Zhao, John Wang and Ruofei Hao
67. Approaches to Missing Data in the Analysis of SpondyloArthritis International Society (ASAS 20) Response and the Creation of the Related CDISC Compliant Analysis Datasets
Christine Joy Dureza
68. SAS® Tools for Working with Dataset-XML files
Lex Jansen
77. Hands-On ADaM ADAE Development
Sandra Minjoe
Programming Techniques
01. Configuring SAS® Business Intelligence (BI) client with the SAS® server to support multilingual data
Wei Zheng
02. Fifty Shades of Sorting
Haibin Shu, Elena Rojco and John He
12. An Excel Macro for Quick and Efficient Analysis of SAS® Log Messages
(No paper available)
Lingyun Chen and Li Cheng
13. A Macro to Add Variables to SDTM Standard Domains
Xianhua Zeng
14. It’s Not Just Fast Merging, It’s Powerful Hashing
Mijun Hu
15. Perl Regular Expressions - A Powerful Tool to Manage Text String
(No paper available)
Weston Chen
17. Creating Binary Tables in a Snap
Yan LIU
23. An efficient way to manipulate huge number of program files in a project
(No paper available)
Long Fang
26. A macro to re-size character variable length
Jianjun Tan and Eric Liao
44. Seamless Data Exchange between SAS and MS Word Documents Through the Integration of VBS in SAS Programs
(No paper available)
JIA YANG and Stanley Wei
45. An approach to fostering an environment of good programming
James Gallagher and Nancy Ni
46. Novel Programming Methods for Change from Baseline Calculations
(No paper available)
Mina Chen and Peter Eberhardt
47. Handling multiple y axes using SAS® Graphs
Mina Chen and Peter Eberhardt
48. Saving Typing with SAS® Editor Abbreviations
Mina Chen
50. The loop within: A macro on looping variables and observations
Eduard Joseph Siquioco
51. A Macro to Automatically Select Covariates from Prognostic Factors and Exploratory Factors for Multivariate Cox PH Model
Yu Cheng
55. A Multi-processing Tool to Batch Submit a List of Programs with Real Time Feedback and Dashboard Email Notification
Huashan Huo and Fanyu Li
69. Effectively Utilizing Loops and Arrays in the DATA Step
Arthur Li
70. SAS Longitudinal Data Techniques - From Change from Baseline to Change from Previous Visits
Chao Wang
71. Using GSUBMIT command to customize the interface in SAS®
xin wang
73. A customized tool for systematic input/output dependency diagnose
Chunlan Xing and Chao Wang
74. Application of Output Delivery System in Creating Customized Targets
Yuan Wang
Statistics including Pharmacokinetics
07. Hands-on Tutorial for Propensity Score Methods in Pharmaceutical Research Using SAS®
(No paper available)
Qinlei Huang
08. Hands-on Tutorial for Piecewise Linear Mixed-effects Models Using SAS® PROC MIXED
Qinlei Huang
11. Why Statistical Analysis Plan (SAP) should be comprehensive.
Riddhi Merchant and Ranjith Prayankotveettil
35. Comparison of Three Methods in Calculating Confidence Intervals for Rate Differences in Non-inferior Clinical Trials
yaohua huang
56. Survival Plots using SAS PROC LIFETEST, GPLOT, and SGPLOT: What are their difference?
Ka Chun CHONG and Chung Ying Zee
57. The Application of Tolerance Interval in Defining Drug Response for Biomarker
Jing Pan
58. Use of SAS® for Risk-Based Monitoring of Survival Endpoints and Adverse Event Data in Clinical Trials
Zhizhuo Zhang, Sichan Tang, Ka Chun CHONG and Chung Ying Zee
61. Clinical trials optimization: Monte Carlo Simulation modeling and SAS applications
Ye Meng