PHUSE SDE2014presentation·SDE·Single Day Event
Data Transparency: Important Considerations for Data De-identification and Sharing Platform COPENHAGEN01 EU · Copenhagen
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PHUSE SDE2014presentation·SDE·Single Day Event
Clinical Trial Data Transparency: Current Progress and Moving Towards One Multi-sponsor Environment COPENHAGEN02 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
Clinical Study Data Processes @ Leo Pharma COPENHAGEN04 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
How Do You Use Look-up Tables COPENHAGEN05 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
Challenges with the interpretation of CDISC: Who can we trust? COPENHAGEN06 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
CDISC Study Data Set-XML: Leaving the Stone Age of data transmission COPENHAGEN07 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
Linked Data: What it is and the potential use in Pharmaceutical Programming COPENHAGEN08 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
What are the Issues from a Regulated Point of View in Relation to use Cloud Solutions? COPENHAGEN09 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
Moving to SAS Drug Development 4 COPENHAGEN10 EU · Copenhagen
PHUSE SDE2014presentation·SDE·Single Day Event
Welcome & Introduction by Event Co-Chairs DURHAM00 US · Durham
PHUSE SDE2014presentation·SDE·Single Day Event
What a Lead Programmer Does for Effective Project Management of Programming Activities under Various Outsourced Models DURHAM01 US · Durham
PHUSE SDE2014presentation·SDE·Single Day Event
Working Model for Effective Functional Service Provider, FSP Collaboration DURHAM03 US · Durham
PHUSE SDE2014presentation·SDE·Single Day Event
CDISC Standards when Programming is Outsourced, Managing Difference of Opinion/Interpretation DURHAM04 US · Durham
PHUSE SDE2014presentation·SDE·Single Day Event
Quality Assurance of Outsourced Programming DURHAM05 US · Durham
PHUSE SDE2014presentation·SDE·Single Day Event
Involvement of Programming in Clinical Trials Disclosure on ClinicalTrials.gov – conclusions and outlook FRANKFURT01 EU · Frankfurt
PHUSE SDE2014presentation·SDE·Single Day Event
Lead Statistical Programmer interacting and meeting face-to-face with the FDA – experiences from an oncology filing and recommendations FRANKFURT02 EU · Frankfurt
PHUSE SDE2014presentation·SDE·Single Day Event
Reengineering a Standard process from Single to Environment Macro Management FRANKFURT03 EU · Frankfurt
PHUSE SDE2014presentation·SDE·Single Day Event
AirTracer – Lighten up clinical trial analysis FRANKFURT04 EU · Frankfurt
PHUSE SDE2014presentation·SDE·Single Day Event
SAS Drug Development in action: efficient standards libraries and study management modules together called CDMation FRANKFURT06 EU · Frankfurt