PHUSE2012·Connect·Regulatory Environment
Cost Effective Standards Implementation: A New Paradigm for the Drug Development Life Cycle RG03 EU · Budapest
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Conference Papers
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PHUSE2012·Connect·Regulatory Environment
Centralised Risk-based Source Data Verification RG04 EU · Budapest
PHUSE2012·Connect·Regulatory Environment
"Bertha.sas" - User Friendly Ways to get Traceability RG05 EU · Budapest
PHUSE2012·Connect·Technology & Applications
MACUMBA - A Modern SAS GUI - Debugging Made Easy AD01 EU · Budapest
PHUSE2012·Connect·Technology & Applications
Testing in the Cloud. Not Just for the Birds, but Monkeys Too AD02 EU · Budapest
PHUSE2012·Connect·Technology & Applications
A Maestro for Our Clinical Data... (Sanofi Clinical Data Warehouse) AD05 EU · Budapest
PHUSE2012·Connect·Technology & Applications
SAS 9.3 Migration - A Project Experience AD06 EU · Budapest
PHUSE2012·Connect·Technology & Applications
Using Workflows to Standardize Business Processes and Best Practices in Pharmaceutical Programming AD07 EU · Budapest
PHUSE2012·Connect·Technology & Applications
East6: Software for Designing, Simulating and Monitoring Group Sequential Trials SD01 EU · Budapest
PHUSE2012·Connect·Technology & Applications
Reveal: Web-Based Software for the Unique Challenges of Enterprise Clinical Data Search SD02 EU · Budapest
PHUSE2012·Connect·Technology & Applications
SAS Drug Development 4.1 - Clinical Programming and Workflow SD04 EU · Budapest
PHUSE2012·Connect·Technology & Applications
Master Data Management and Possible Applications for Clinical Trial Data SD06 EU · Budapest
PHUSE2012·Connect·Technology & Applications
SAS Clinical Standards Toolkit 1.5 - How Do I Know My Metadata is Right? TS01 EU · Budapest
PHUSE2012·Connect·Technology & Applications
Let SAS Handle your CDISC Compliance Check: Automating OpenCDISC Validator in SAS TS04 EU · Budapest