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Min Chen

22 papers and 1 presentation; 22 titles; 10 coauthors.

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Conference × Year × Title × Co-authors Extras Pages
PharmaSUG 2024 A New Approach to Automating the Creation of the Subject Visits (SV) Domain Xiangchen (Bob) Cui,
Jessie Wang		 source 24
PharmaSUG 2024 A Practical Approach to Automating SDTM Using a Metadata-Driven Method That Leverages CRF Specifications and SDTM Standards Xiangchen (Bob) Cui,
Jessie Wang		 source 23
PHUSE US 2024 A Practical Approach to Automating SDTM Using a Metadata-Driven Method that Leverages eCRF Specifications and SDTM Programming Standards Xiangchen (Bob) Cui source
presentation source		 12
PharmaSUG 2019 Automate the Process to Ensure the Compliance with FDA Business Rules in SDTM Programming for FDA Submission Xiangchen (Bob) Cui,
Hao Guan,
Letan (Cleo) Lin		 source 16
MWSUG 2018 Handling Missing Data in Exploratory Factor Analysis Using SAS 3
PharmaSUG 2017 Leveraging Study Data Reviewer-s Guide (SDRG) in Building FDA-s Confidence in Sponsor-s Submitted Datasets Xiangchen (Bob) Cui,
Letan (Cleo) Lin		 source 10
MWSUG 2016 The Power of Cumulative Distribution Function (CDF) Plot in Assessing Clinical Outcomes Patricia Kultgen 6
PharmaSUG 2016 A Practical Approach to Re-sizing Character Variable Lengths for FDA Submission Datasets (both SDTM and ADaM) Xiangchen (Bob) Cui source 19
PharmaSUG 2016 A SAS Macro Tool to Automate Generation of Define.xml V2.0 from SDTM Specification for FDA Submission Xiangchen (Bob) Cui source 24
PharmaSUG 2016 Automatic Consistency Checking of Controlled Terminology among SDTM Datasets, Define.xml, and NCI/CDISC Controlled Terminology for FDA Submission Xiangchen (Bob) Cui source 13
PharmaSUG 2015 A Methodology of Laboratory Data Reporting of Potentially Clinical Significant Abnormality (PCSA) for Clinical Study Report Xiangchen (Bob) Cui source 21
PharmaSUG 2015 A SAS Macro Tool to Automate Generation of Define.xml V2.0 from ADaM Specification for FDA Submission Xiangchen (Bob) Cui source 28
SGF 2013 A Preventive Approach for Automatic Checking of CDISC ADaM Metadata to Detect Noncompliance [presentation] Xiangchen (Bob) Cui,
Tathabbai Pakalapati		 source 2
PharmaSUG 2012 An Innovative ADaM Programming Tool for FDA Submission Xiangchen (Bob) Cui,
Tathabbai Pakalapati		 source 25
PharmaSUG 2012 Automatic Consistency Checking of Controlled Terminology and Value Level Metadata between ADaM Datasets and Define.xml for FDA Submission Xiangchen (Bob) Cui source 15
PharmaSUG 2012 Automatic Detection and Identification of Variables with All Missing Values in SDTM/ADaM Datasets for FDA Submission Xiangchen (Bob) Cui source 7
PharmaSUG 2012 Automatic Version Control and Track Changes of CDISC ADaM Specifications for FDA Submission Xiangchen (Bob) Cui source 8
SGF 2012 Automatic Consistency Checking of Controlled Terminology and Value Level Metadata between ADaM Datasets and Define.xml for FDA Submission Xiangchen (Bob) Cui source 15
SESUG 2011 Development of a SAS Macro for Automated Data Cleaning of Major Outcomes of Interest in Hematopoietic Cell Transplantation Peigang Li,
Zhiwei Wang		 source 7
PharmaSUG 2011 A Cost-Effective SDTM Conversion for NDA Electronic Submission Xiangchen (Bob) Cui,
Scott E. Moseley		 source 12
PharmaSUG 2011 Automating the Process of Preparing Data Definition Document for NDA Electronic Submission from Programming Specification in Word Format Xiangchen (Bob) Cui,
Scott E. Moseley		 source 12
PharmaSUG 2011 New Tips and Tricks for Creating a Harmonized, Report-Friendly SDTM and ADaM Lab Data for a Clinical Study Report Xiangchen (Bob) Cui,
Scott E. Moseley		 source 12
MWSUG 2010 Tips for Automating Univariate Outcomes Analysis in Hematopoietic Stem Cell Transplantation Peigang Li,
Xiaochun Zhu		 7

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