Pharmaceutical Programming

SAS code for the estimation and between-group comparison of cumulative incidence functions in competing risks survival analysis
pp. 1-13(13)
Author: Bond, Simon

PROC MIXED and early phase trials
pp. 14-18(5)
Author: Fordred, Shelley

Application of component-wise rank method to bivariate bioequivalence case
pp. 19-23(5)
Authors: Nandakumar, Srinand P.; McKean, Joseph W.

Producing comprehensive integrated summaries
pp. 24-27(4)
Author: Whitworth, Michael

Streamlining the PK/PD data transfer process — 1 year later
pp. 28-30(3)
Authors: Collins, Arthur; Silva, Greg

Impact of daylight saving time shifts on data quality of a pharmacokinetic study
pp. 31-34(4)
Author: Ahrweiler, Sascha

Remapping of codes (and decodes) in analysis datasets for electronic submissions
pp. 35-38(4)
Author: Guettner, Joerg

How do we ensure the programmers we have today will meet the business needs of tomorrow?
pp. 39-44(6)
Authors: Leigh, Christine; Rowe, Karen

Much ADaM about nothing — a proc away in a day
pp. 45-50(6)
Authors: Endri,; Hale, Rowland

A SAS macro to check SDTM domains against controlled terminology
pp. 51-58(8)
Author: Wendland, Guido

Tracing data elements through a standard data flow
pp. 59-69(11)
Author: Dootson, Alistair

SAS dataset utility with excel output
pp. 70-73(4)
Author: Horton, Rob

Use of ODS tagsets.excelxp to create excel type files
pp. 74-80(7)
Author: Staddon, Douglas

Aspects of software development
pp. 81-84(4)
Authors: Glaß, Katja

Unit testing as a cornerstone of SAS application development
pp. 85-90(6)
Authors: Di Tommaso, Dante; Roche, F. Hoffmann-La

Different methods of calculating body sway area
pp. 91-106(16)
Author: Wollseifen, Thomas

Introduction to numeric precision and representation issues: why 4.8 minus 4.6 is not always equal to 0.2
pp. 107-113(7)
Author: Tambascia, Nicola

Preparing an eSubmission based on multiple trials, some of which are ongoing — challenges for statistical programming
pp. 114-118(5)
Authors: Carlsheimer, Åsa