PharmaSUG2017paper·US·Statistics & Pharmacokinetics
Multiple Imputation: A Statistical Programming Story SP01
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PharmaSUG2017paper·US·Statistics & Pharmacokinetics
Multiplicity Controlled Analyses Using SAS/IML SP02
PharmaSUG2017paper·US·Statistics & Pharmacokinetics
Population PK/PD Analysis – SAS® with R and NONMEM® Make Customization Easy SP04
PharmaSUG2017paper·US·Statistics & Pharmacokinetics
Combining Survival Analysis Results after Multiple Imputation of Censored Event Times SP05
PharmaSUG2017paper·China·Statistics & Pharmacokinetics
Time-Dependent Covariates 'Survival' More in PROC PHREG SP-01 Shanghai
PharmaSUG2017paper·China·Statistics & Pharmacokinetics
Receiver Operating Characteristic (ROC) Curve Analysis using SAS SP-02 Shanghai
PharmaSUG2017paper·China·Statistics & Pharmacokinetics
Clinical PK-PD Model: Problems and Countermeasures SP-03 Shanghai
PharmaSUG2017paper·China·Statistics & Pharmacokinetics
Visualization & interactive application in design and analysis by using Rshiny SP-04 Shanghai
PharmaSUG2017paper·China·Statistics & Pharmacokinetics
A Path to Gain Confidenct with your Confidence Interval in Clinical Trial Analysis SP-05 Shanghai
PharmaSUG2017paper·China·Statistics & Pharmacokinetics
%ScoreQoL: SAS Macro-Program that Automates the Scoring of Quality of Life Questionnaires SP-06 Shanghai
PharmaSUG2017paper·US·Submission Standards
Preparing Analysis Data Model (ADaM) Data Sets and Related Files for FDA Submission SS02
PharmaSUG2017paper·US·Submission Standards
Use of Traceability Chains in Study Data and Metadata for Regulatory Electronic Submission SS03
PharmaSUG2017paper·US·Submission Standards
Good versus better SDTM: Including Screen Failure Data in the Study SDTM? SS04
PharmaSUG2017paper·US·Submission Standards
Awareness from Electronic Data Submission to PMDA and FDA — Lesson & Learnt from hands-on experiences — SS06
PharmaSUG2017paper·US·Submission Standards
Overview and Application of the HCV Vertical Resistance Analysis Template SS07
PharmaSUG2017paper·US·Submission Standards
Creating Define-XML version 2 including Analysis Results Metadata with the SAS® Clinical Standards Toolkit SS08
PharmaSUG2017paper·US·Submission Standards
Leveraging Study Data Reviewer’s Guide (SDRG) in Building FDA’s Confidence in Sponsor’s Submitted Datasets SS09