Pharmaceutical Programming

Titel Veröffentlichungsdatum Sprache Zitate
Result disclosure on ClinicalTrials. gov — first experiences and challenges2010/12/01English20
Streamlining the PK/PD data transfer process2010/06/01English2
Evolution and Implementation of the CDISC Study Data Tabulation Model (SDTM)2008/08/01English1
Developing SAS®standard macros with variable argument techniques2008/12/01English
Creating macros for survival data in oncology study2008/12/01English
Workflow: defining, designing and building a programming process and version control system. Part I – history and background2008/08/01English
Lessons learned: valuable (but hidden) SAS®details2008/08/01English
How to get 10 pounds of data into a 5-pound can – using flyover technique In HTML output2008/08/01English
Implementing CFR 21 part 11 for SAS®without tears or joins2008/12/01English
Design of eCRFs in consideration of subsequent data analysis2008/12/01English
A CDISC SDTM model for the medical device and diagnostic industry2008/08/01English
A ‘systematic review’ of PhUSE: what PhUSE users made available to the public after three years2008/08/01English
Calculating medication compliance, adherence and persistence in administrative pharmacy claims databases2008/08/01English
Techniques for writing robust SAS®macros2009/08/01English
XML for SAS®programmers2009/08/01English
Visual guide to clinical programming with SAS®2009/08/01English
Editorial2009/08/01English
Using SAS®9 in clinical research2009/08/01English
The Submission Data File System: automating the creation of CDISC SDTM and ADaM datasets2009/08/01English
The Italian post-marketing registries2012/12/01English
MACUMBA — a modern SAS GUI — debugging made easy2012/12/01English
The dataset generation for survival analysis with the ADaM Basic Data Structure for Time-to-Event Analyses (ADTTE) standard2012/12/01English
A peak at PK — an introduction to pharmacokinetics2012/12/01English
Bootstrap simulations to estimate overall survival based on the distribution of a historical control2012/12/01English
Programming challenges of sampling controls to cases from the dynamic risk sets in nested case–control studies2012/12/01English
Merging RTF files using SAS®, MSWord®, and Acrobat Distiller®2012/12/01English
Approaches to creating ADaM subject-level analysis datasets (ADSL) for integrated analyses2012/12/01English
Controlling OpenCDISC validator using R2012/12/01English
The use of checksums to ensure data integrity in the healthcare industry2012/12/01English
Processing of hierarchical data with hash objects Part 1 – Creation of XML documents2012/12/01English